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133157-01-4

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133157-01-4 Usage

Description

(S)-METHYL 2-(DIPHENYLMETHYLENEAMINO)-3-HYDROXYPROPANOATE is a chiral chemical compound with the molecular formula C19H19NO3, derived from the amino acid phenylalanine. It is commonly used in organic synthesis and medicinal chemistry due to its unique chemical structure and properties.

Uses

Used in Pharmaceutical Industry:
(S)-METHYL 2-(DIPHENYLMETHYLENEAMINO)-3-HYDROXYPROPANOATE is used as a building block in the synthesis of pharmaceutical drugs and other organic compounds. Its chiral nature allows for the creation of enantiomers, which can have different biological activities and properties.
Used in Drug Development:
(S)-METHYL 2-(DIPHENYLMETHYLENEAMINO)-3-HYDROXYPROPANOATE is used in drug development for its potential applications in creating new pharmaceutical compounds. Its unique structure and properties make it a valuable asset in the design and synthesis of novel drugs with specific therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 133157-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,1,5 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133157-01:
(8*1)+(7*3)+(6*3)+(5*1)+(4*5)+(3*7)+(2*0)+(1*1)=94
94 % 10 = 4
So 133157-01-4 is a valid CAS Registry Number.

133157-01-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2S)-2-(benzhydrylideneamino)-3-hydroxypropanoate

1.2 Other means of identification

Product number -
Other names Methyl N-(Diphenylmethylene)-L-serinate

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:133157-01-4 SDS

133157-01-4Relevant articles and documents

Aluminoxy acetals from α-amino esters: Chirality transfer via sequential addition of hydride and C-nucleophiles. 2-amino alcohols and sphingosines

Polt,Peterson,DeYoung

, p. 5469 - 5480 (2007/10/02)

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O-Glycopeptides: A simple β-stereoselective glycosidation of serine and threonine via a favorable hydrogen bonding pattern

Szabo,Li,Polt

, p. 585 - 588 (2007/10/02)

Glycosidation of serine and threonine is promoted by using an intramolecular hydrogen bond to the hydroxyl group.

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