Welcome to LookChem.com Sign In|Join Free

CAS

  • or

133157-01-4

Post Buying Request

133157-01-4 Suppliers

Recommended suppliersmore

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

133157-01-4 Usage

General Description

(S)-Methyl 2-(diphenylmethyleneamino)-3-hydroxypropanoate is a chemical compound with the molecular formula C19H19NO3. It is a derivative of the amino acid phenylalanine, and it is commonly used in organic synthesis and medicinal chemistry. (S)-METHYL 2-(DIPHENYLMETHYLENEAMINO)-3-HYDROXYPROPANOATE is a chiral molecule, meaning it has two enantiomers that are mirror images of each other. It is often used as a building block in the synthesis of pharmaceutical drugs and other organic compounds. The compound has potential applications in drug development and the pharmaceutical industry due to its unique chemical structure and properties.

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)

-

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.

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

What can I do for you?
Get Best Price

Get Best Price for 133157-01-4