What is the Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)-?

Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)- is , while it's Molecular Formula is C14H15NO4S. Used in Pharmaceutical Research: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is used as a reagent in pharmaceutical research for its ability to act as a nucleophile and a base, facilitating various chemical reactions and the synthesis of new compounds. Used in Organic Synthesis: In the field of organic synthesis, Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is employed as a key intermediate, enabling the creation of a wide range of organic compounds. Used in Anti-inflammatory Applications: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is used as an anti-inflammatory agent, potentially providing relief from inflammation and associated symptoms. Used in Anti-cancer Applications: In preclinical studies, Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)has shown potential as an anti-cancer agent, offering a promising avenue for the development of new cancer treatments. Used in Drug Production: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is used as a starting material in the production of various pharmaceutical drugs, contributing to the development of new medications. Used in Agrochemical Production: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is also utilized in the production of agrochemicals, where it serves as a starting material for the synthesis of various agricultural chemicals.

What is the CAS number for Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)-?

The CAS number of Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)- is 123664-84-6.

What is Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)- (123664-84-6) used for?

Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)-, also known as a sulfonamide derivative, is a chemical compound characterized by the molecular formula C14H15NO4S. It features methoxy and phenoxy substituents on the nitrogen atom, which contribute to its unique chemical properties. This versatile compound is widely utilized in organic synthesis and pharmaceutical research, where it serves as both a nucleophile and a base. Its potential as an anti-inflammatory and anti-cancer agent has been recognized in preclinical studies, and it is also employed as a starting material in the production of pharmaceutical drugs and agrochemicals. Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)holds significant importance in medicinal chemistry and drug development due to its diverse range of biological activities and applications.

What is the Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)-?

Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)- is , while it's Molecular Formula is C14H15NO4S. Used in Pharmaceutical Research: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is used as a reagent in pharmaceutical research for its ability to act as a nucleophile and a base, facilitating various chemical reactions and the synthesis of new compounds. Used in Organic Synthesis: In the field of organic synthesis, Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is employed as a key intermediate, enabling the creation of a wide range of organic compounds. Used in Anti-inflammatory Applications: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is used as an anti-inflammatory agent, potentially providing relief from inflammation and associated symptoms. Used in Anti-cancer Applications: In preclinical studies, Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)has shown potential as an anti-cancer agent, offering a promising avenue for the development of new cancer treatments. Used in Drug Production: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is used as a starting material in the production of various pharmaceutical drugs, contributing to the development of new medications. Used in Agrochemical Production: Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)is also utilized in the production of agrochemicals, where it serves as a starting material for the synthesis of various agricultural chemicals.

What is the CAS number for Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)-?

The CAS number of Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)- is 123664-84-6.

What is Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)- (123664-84-6) used for?

Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)-, also known as a sulfonamide derivative, is a chemical compound characterized by the molecular formula C14H15NO4S. It features methoxy and phenoxy substituents on the nitrogen atom, which contribute to its unique chemical properties. This versatile compound is widely utilized in organic synthesis and pharmaceutical research, where it serves as both a nucleophile and a base. Its potential as an anti-inflammatory and anti-cancer agent has been recognized in preclinical studies, and it is also employed as a starting material in the production of pharmaceutical drugs and agrochemicals. Methanesulfonamide, N-(5-methoxy-2-phenoxyphenyl)holds significant importance in medicinal chemistry and drug development due to its diverse range of biological activities and applications.

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Product classification

123664-84-6

Product Name：N - (5-methoxy-2-phenoxyphenyl) methanesulfonamide (Imorad intermediate 3)
Molecular Formula：C14H15NO4S
Purity：99%
Molecular Weight：293.343

Inquiry

Product Details

Purity:99%

China cas 123664-84-6 manufacturer wholesale N - (5-methoxy-2-phenoxyphenyl) methanesulfonamide (Imorad intermediate 3) at affordable price

Molecular Formula:C14H15NO4S
Molecular Weight:293.343
Boiling Point:411.4±55.0 °C(Predicted)
PKA:8.07±0.10(Predicted)
PSA：73.01000
Density:1.306±0.06 g/cm3(Predicted)
LogP:4.01280

123664-84-6 Relevant articles

Iguratimod intermediate and synthesis method thereof

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Paragraph 0036; 0039; 0042, (2019/05/15)

The invention belongs to the technical f...

Synthesis and antiinflammatory activity of 7-methanesulfonylamino-6- phenoxychromones. Antiarthritic effect of the 3-formylamino compound (T-614) in chronic inflammatory disease models

Inaba, Takihiro,Tanaka, Keiichi,Takeno, Ryuko,Nagaki, Hideyoshi,Yoshida, Chosaku,Takano, Shuntaro

, p. 131 - 139 (2007/10/03)

A group of derivatives of 7-methanesulfo...

4H-1-benzopyran-4-one derivative or its salt, process for producing the same and pharmaceutical composition comprising the same as active ingredient

-

, (2008/06/13)

This invention relates to a 4H-1-benzopy...

123664-84-6 Process route

: 76838-72-7
5-methoxy-2-phenoxyaniline

: 124-63-0
methanesulfonyl chloride

: 123664-84-6
N-(5-methoxy-2-phenoxyphenyl)methanesulfonamide

Conditions

Conditions	Yield
With hydrogenchloride; In pyridine; water; ethyl acetate;	91.9%
With pyridine; at 20 ℃; for 1h;	82%
With pyridine; at 5 - 30 ℃; for 1.5h; Temperature; Green chemistry;	276.47 g

: 84594-95-6
5-methoxy-1-nitro-2-phenoxybenzene

: 123664-84-6
N-(5-methoxy-2-phenoxyphenyl)methanesulfonamide

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 72 percent / 4N aq. HCl; Fe / ethanol / 0.33 h / 65 - 70 °C 2: 82 percent / pyridine / 1 h / 20 °C With pyridine; hydrogenchloride; iron; In ethanol; 1: Reduction / 2: Mesylation;

123664-84-6 Upstream products

76838-72-7
5-methoxy-2-phenoxyaniline
124-63-0
methanesulfonyl chloride
84594-95-6
5-methoxy-1-nitro-2-phenoxybenzene
10298-80-3
2-chloro-5-methoxynitrobenzene

123664-84-6 Downstream products

149436-41-9
α-amino-2-methoxy-4-methanesulfonamido-5-phenoxyacetophenone hydrochloride
123664-55-1
ethyl 2-(2-benzyloxy-4-methylsulfonylamino-5-phenoxybenzoyl)acetate
123664-56-2
ethyl 3-[2-hydroxy-4-[(methylsulfonyl)amino]-5-phenoxyphenyl]-3-oxopropanoate
123663-68-3
ethyl 7-[(methylsulfonyl)amino]-4-oxo-6-phenoxy-4H-3-chromenecarboxylate

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