Welcome to LookChem.com Sign In|Join Free
  • or
Methyl 5-amino-2-methoxy-4-methylbenzoate, also known as Methyl 5-amino-salicylate, is a chemical compound that belongs to the class of benzoic acid derivatives. It is commonly used in the production of pharmaceuticals, particularly as an intermediate in the synthesis of various drugs. Methyl 5-amino-2-methoxy-4-methylbenzoate is also known for its ability to act as an anti-inflammatory and analgesic agent. It has been evaluated for its potential therapeutic effects in the treatment of various conditions such as inflammation, pain, and other related disorders.

70752-21-5

Post Buying Request

70752-21-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

70752-21-5 Usage

Uses

Used in Pharmaceutical Industry:
Methyl 5-amino-2-methoxy-4-methylbenzoate is used as an intermediate in the synthesis of various drugs for its versatile chemical properties and potential therapeutic effects.
Used in Cosmetic and Personal Care Industry:
Methyl 5-amino-2-methoxy-4-methylbenzoate is used as an anti-inflammatory agent for its potential applications in cosmetic and personal care products to help alleviate inflammation and related skin conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 70752-21-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,7,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 70752-21:
(7*7)+(6*0)+(5*7)+(4*5)+(3*2)+(2*2)+(1*1)=115
115 % 10 = 5
So 70752-21-5 is a valid CAS Registry Number.

70752-21-5Relevant academic research and scientific papers

Synthesis and Neuroleptic Activity of N--2-methoxy-5-sulfonamidobenzamides

Ogata, Masaru,Matsumoto, Hiroshi,Kida, Shiro,Shiomi, Teruo,Eigyo, Masami,Hirose, Katsumi

, p. 1137 - 1141 (2007/10/02)

A series of some novel N-benzamides involving replacement of the sulfamoyl group in sulpiride with a sulfonamido group was synthesized and tested for dopamine receptor blockade.In comparison with sulpiride, several compounds were considerably more potent than sulpiride as dopamine receptor blockers.The structure-activity relationships are discussed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 70752-21-5