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4703-32-6

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4703-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4703-32-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4703-32:
(6*4)+(5*7)+(4*0)+(3*3)+(2*3)+(1*2)=76
76 % 10 = 6
So 4703-32-6 is a valid CAS Registry Number.

4703-32-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-2-[N-(4-methylphenyl)sulfonylamino]-3-(4-hydroxyphenyl) propionic acid

1.2 Other means of identification

Product number -
Other names Ts-Tyr-OH

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4703-32-6 SDS

4703-32-6Downstream Products

4703-32-6Relevant articles and documents

Development of amino acid conjugated sulfonamides as potent antiulcer agent

Sahoo, Shakti Prasanna,Subudhi, Bharat Bhusan

, p. 3039 - 3048 (2014/05/06)

A series of 2-{[(4-methylphenyl) sulfonyl] amino}-3-sulfanylpropanoic acid (1a) and its analogs 1b-j have been synthesized. These compounds were screened for their in vivo efficacy in pyloric ligation model. Compounds 1a and 1b with higher antiulcer potential were further screened in other gastric models to explore the mode of antiulcer action. To further understand the mode of action, in vitro inhibition of H+/K+ ATPase activity in gastric microsome isolated from rat stomach was studied. This was rationalized by in silico experiments.

HIV protease inhibitors based on amino acid derivatives

-

, (2008/06/13)

A compound selected from the group consisting of a compound of formula I 1a compound of formula II 2and when the compound of formula I and II comprises an amino group pharmaceutically acceptable ammonium salts thereof, wherein R1, R2, Cx, n, R3, R4, R5, Y are as defined in the specification.

Total synthesis of FR901483

Ousmer, Malika,Braun, Norbert A.,Ciufolini, Marco A.

, p. 765 - 767 (2007/10/03)

The total synthesis of FR901483, a structurally novel immunosuppressant, has been accomplished by the use of technology recently developed in this laboratory for the oxidative cyclization of phenolic oxazolines to spirolactams. Our approach may reflect th

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