135934-38-2

• 

• Basic information

  1. Product Name: Benzenepropanoic acid, a-[[(4-methyl-1-piperazinyl)sulfonyl]methyl]-, (S)-
  2. Synonyms:
  3. CAS NO:135934-38-2
  4. Molecular Formula: C15H22N2O4S
  5. Molecular Weight: 326.417
  6. EINECS: N/A
  7. Product Categories: N/A
  8. Mol File: 135934-38-2.mol
  9. Article Data: 4

• Chemical Properties

  1. Melting Point: N/A
  2. Boiling Point: N/A
  3. Flash Point: N/A
  4. Appearance: N/A
  5. Density: N/A
  6. Refractive Index: N/A
  7. Storage Temp.: N/A
  8. Solubility: N/A
  9. CAS DataBase Reference: Benzenepropanoic acid, a-[[(4-methyl-1-piperazinyl)sulfonyl]methyl]-, (S)-(CAS DataBase Reference)
  10. NIST Chemistry Reference: Benzenepropanoic acid, a-[[(4-methyl-1-piperazinyl)sulfonyl]methyl]-, (S)-(135934-38-2)
  11. EPA Substance Registry System: Benzenepropanoic acid, a-[[(4-methyl-1-piperazinyl)sulfonyl]methyl]-, (S)-(135934-38-2)

• Safety Data

  1. Hazard Codes: N/A
  2. Statements: N/A
  3. Safety Statements: N/A
  4. WGK Germany:
  5. RTECS:
  6. HazardClass: N/A
  7. PackingGroup: N/A
  8. Hazardous Substances Data: 135934-38-2(Hazardous Substances Data)

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• Benzenepropanoic acid, a-[[(4-methyl-1-piperazinyl)sulfonyl]methyl]-, (S)-

  Cas No: 135934-38-2

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135934-38-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 135934-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,9,3 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135934-38:
(8*1)+(7*3)+(6*5)+(5*9)+(4*3)+(3*4)+(2*3)+(1*8)=142
142 % 10 = 2
So 135934-38-2 is a valid CAS Registry Number.

135934-38-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	(2S) 2-Benzyl-3-(1-methyl-piperazin-4-ylsulfonyl)propionic Acid

1.2 Other means of identification

Product number	-
Other names	2(S)2-Benzyl-3-(4-methyl-piperazin-1-ylsulfonyl) propionic acid

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:135934-38-2 SDS

135934-38-2Upstream product

• 147794-61-4 2-Benzyl-3-(morpholine-4-sulfonyl)-propionic acid methyl ester 
• 138742-44-6 methyl 2-Benzyl-3-(4-methyl-piperazin-1-ylsulfonyl)propionate 
• 18020-59-2 methyl 3-hydroxy-2-methylidene-3-phenylpropionate 
• 100-52-7 benzaldehyde 
• 103669-71-2 (Z)-methyl 2-(bromomethyl)-3-phenylacrylate 
• 135934-36-0 methyl 2-benzyl-3-(chlorosulfonyl)propionate 

135934-38-2Downstream Products

135934-38-2Relevant articles and documents

ENCAPSULATED RENIN INHIBITOR COMPOSITION

-

, (2008/06/13)

A pharmaceutical composition comprising a solution of a tenin inhibitor of the formula: STR1 wherein R 1 is 4-piperazinyl, 1-methyl-4-piperazinyl, 1-methyl-1-oxo-4-piperazinyl, 2-oxo-4-piperazinyl, 4-morpholinyl, 4-thiomorpholinyl or 1-methyl-4-homopiperazinyl; R 2 is benzyl, p-methoxybenzyl, 2-phenylethyl, 1-naphthylmethyl or 2-naphthylmethyl;R 3 is 4-thiazolyl, 2-amino-4-thiazolyl, 2-thiazolyl, 5-thiazolyl, 1-pyrazolyl, 3-pyrazolyl, 1-imidazolyl, n-propyl, isopropyl, CH 3 S--or CH 3 SCH 2--;R 4 is loweralkyl or cyclopropyl;R 5 is hydrogen or loweralkyl; andX is CH 2 or NH; or a pharmaceutically acceptable salt, ester or prodrug thereof in a pharmaceutically acceptable solvent, said solution being encapsulated in a soft elastic gelatin capsule.

Enzyme-catalyzed synthesis of optically pure β-sulfonamidopropionic acids. Useful starting materials for P-3 site modified renin inhibitors

Mazdiyasni, Hormoz,Konopacki, Donald B.,Dickman, Daniel A.,Zydowsky, Thomas M.

, p. 435 - 438 (2007/10/02)

The novel and efficient of several racemic β-sulfonamidopropionate esters is described. Treatment of the racemic esters with Chymotrypsin or Subtilisin Carlsberg (purified of detergent grade) provided the corresponding (S)-carboxylic acids in 60-90% yield

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