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118872-62-1

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118872-62-1 Usage

Uses

The preparation and synthesis of deuteriated organic compound, 4-Aminobenzoic-2,6-d2 Acid. It is reported as a stable isotope-labeled folate internal standard for the measurement of red blood cell folates using gas chromatography-mass spectrometry.

Check Digit Verification of cas no

The CAS Registry Mumber 118872-62-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,8,7 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 118872-62:
(8*1)+(7*1)+(6*8)+(5*8)+(4*7)+(3*2)+(2*6)+(1*2)=151
151 % 10 = 1
So 118872-62-1 is a valid CAS Registry Number.

118872-62-1SDS

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 4-AMINOBENZOIC-2,6-D2 ACID

1.2 Other means of identification

Product number -
Other names P-AMINO-DL-PHENYLALANINE 1-HYDRATE

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:118872-62-1 SDS

118872-62-1Upstream product

118872-62-1Downstream Products

118872-62-1Relevant articles and documents

Convenient and efficient deuteration of functionalized aromatics with deuterium oxide: Catalysis by cycloocta-1,5-dienyliridium(I) 1,3-dionates

McAuley,Hickey,Kingston,Jones,Lockley,Mather,Spink,Thompson,Wilkinson

, p. 1191 - 1204 (2003)

Aromatic compounds bearing an ortho-directing substituent may be deuterated by exchange with deuterium oxide in the presence of a range of cycloocta-1,5-dienyliridium(I)1,3-dionate catalysts. The exchange takes place in several dipolar aprotic solvents an

Ruthenium(II)-Catalyzed Hydrogen Isotope Exchange of Pharmaceutical Drugs by C?H Deuteration and C?H Tritiation

Müller, Valentin,Weck, Remo,Derdau, Volker,Ackermann, Lutz

, p. 100 - 104 (2019/12/24)

Well-defined ruthenium(II) biscarboxylate complexes enabled selective ortho-deuteration with weakly-coordinating, synthetically useful carboxylic acid with outstanding levels of isotopic labeling. The robust nature of the catalytic system was reflected by

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