Welcome to LookChem.com Sign In|Join Free
  • or
3-Thiazolidinecarboxylic acid, 4-(hydroxymethyl)-2-phenyl-, methyl ester, (2R,4R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64970-80-5

Post Buying Request

64970-80-5 Suppliers

Recommended suppliers

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

64970-80-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64970-80-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,9,7 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 64970-80:
(7*6)+(6*4)+(5*9)+(4*7)+(3*0)+(2*8)+(1*0)=155
155 % 10 = 5
So 64970-80-5 is a valid CAS Registry Number.

64970-80-5SDS

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 (2R,4R)-4-hydroxymethyl-2-phenylthiazolidine-3-carboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 3-Carbomethoxy-4-(R)-hydroxymethyl-2-(R)-phenylthiazolidin

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:64970-80-5 SDS

64970-80-5Relevant academic research and scientific papers

A Facile Synthesis of a Key Intermediate for (+)-Biotin via Strecker Reaction

Mori, Yoshikazu,Kimura, Mayumi,Seki, Masahiko

, p. 2311 - 2316 (2007/10/03)

The Strecker reaction of (2R,4R)-2-phenyl-3-phenoxycarbonylthiazolidine-4- carbaldehyde (4b), which was readily prepared from L-cysteine, with benzylamine and trimethylsilyl cyanide provided α-amino nitrile 5b stereoselectively (syn-anti, 2:1), Amidation of 5b and subsequent cyclization gave bicyclic compound 6, which, upon reduction with zinc dust, hydrolysis and subsequent cyclization, furnished thiolactone 2, a key intermediate for (+)-biotin (1).

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 64970-80-5