Welcome to LookChem.com Sign In|Join Free

CAS

  • or

101312-07-6

Post Buying Request

101312-07-6 Suppliers

Recommended suppliersmore

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

101312-07-6 Usage

General Description

1H-Indole-3-propanoic acid, alpha-hydroxy, (-alpha-R)-(9CI) is a chemical compound that belongs to the family of indole derivatives. It is an alpha-hydroxy acid, which means it contains a hydroxyl group attached to the carbon atom adjacent to the carboxyl group. 1H-Indole-3-propanoicacid,-alpha--hydroxy-,(-alpha-R)-(9CI) has potential biological activities and is believed to have therapeutic properties, especially in the field of medicine. It is often used in pharmaceutical research and drug development due to its ability to modulate various biochemical pathways. However, further studies are required to fully understand its pharmacological and toxicological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 101312-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,3,1 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 101312-07:
(8*1)+(7*0)+(6*1)+(5*3)+(4*1)+(3*2)+(2*0)+(1*7)=46
46 % 10 = 6
So 101312-07-6 is a valid CAS Registry Number.

101312-07-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-hydroxy-3-(1H-indol-3-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 3IL

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:101312-07-6 SDS

101312-07-6Downstream Products

101312-07-6Relevant articles and documents

Biocontrolled formal inversion or retention of L -α-amino acids to enantiopure (R)- or (S)-hydroxyacids

Busto, Eduardo,Grischek, Barbara,Kroutil, Wolfgang,Richter, Nina

supporting information, p. 11225 - 11228,4 (2015/01/07)

Natural L-α-amino acids and L-norleucine were transformed to the corresponding α-hydroxy acids by formal biocatalytic inversion or retention of absolute configuration. The one-pot transformation was achieved by a concurrent oxidation reduction cascade in aqueous media. A representative panel of enantiopure (R)- and (S)-2-hydroxy acids possessing aliphatic, aromatic and heteroaromatic moieties were isolated in high yield (67-85 %) and enantiopure form (>99 % ee) without requiring chromatographic purification.

Formations of (5-Hydroxy)indole S-(-)-lactic Acid, N-acetyl-5-hydroxy-L-tryptophan and (5-Hydroxy)indole Carboxylic Acid in the Metabolism of Tryptophan and 5-Hydroxytryptophan by Chromobacterium violaceum

Hoshino, Tsutomu,Yamamoto, Masahiro,Uchiyama, Takeo

, p. 1609 - 1610 (2007/10/02)

Tryptophan metabolism catalyzing the production of (5-hydroxy)indolelactate, (5-hydroxy)indole carboxylate, and N-acetyl-5-hydroxytryptophan was found in Chromobacterium violaceum.These metabolites have never been reported before.Metabolic pathways from tryptophan and 5-hydroxytryptophan are proposed.

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 101312-07-6