Welcome to LookChem.com Sign In|Join Free

CAS

  • or

27004-49-5

Post Buying Request

27004-49-5 Suppliers

Recommended suppliersmore

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

27004-49-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27004-49-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,0 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 27004-49:
(7*2)+(6*7)+(5*0)+(4*0)+(3*4)+(2*4)+(1*9)=85
85 % 10 = 5
So 27004-49-5 is a valid CAS Registry Number.

27004-49-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium,2-hydroxy-2-(1H-indol-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names Hydroxy-indol-3-yl-essigsaeure,Natrium-Salz

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:27004-49-5 SDS

27004-49-5Upstream product

27004-49-5Downstream Products

27004-49-5Relevant articles and documents

Bioconjugation with Thiols by Benzylic Substitution

Watanabe, Kenji,Ohshima, Takashi

supporting information, p. 3959 - 3964 (2018/02/22)

A benzylic substitution of 3-indolyl(hydroxyl)acetate derivatives with thiols proceeded specifically in the presence of amino, carboxy, and phosphate groups in weakly acidic aqueous solutions under nearly physiological condition, while no reaction occurred at pH over 7. Kinetic studies revealed that the reaction followed second-order kinetics (first-order in the reactant and first-order in thiol) in contrast with the SN1 mechanism of common benzylic substitution of alcohols. The utility of the present method for functionalization of biomacromolecules was demonstrated using several model proteins, such as lysozyme, insulin, trypsin, and serum albumin. The catalytic bioactivity of lysozyme in lysis of Micrococcus lysodeikticus cells was completely retained after the modification.

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 27004-49-5