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151985-13-6

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151985-13-6 Usage

Uses

o-Toluidine-d3 (methyl-d3) can be used to treat diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 151985-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,9,8 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 151985-13:
(8*1)+(7*5)+(6*1)+(5*9)+(4*8)+(3*5)+(2*1)+(1*3)=146
146 % 10 = 6
So 151985-13-6 is a valid CAS Registry Number.

151985-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name O-TOLUIDINE-D3 (METHYL-D3)

1.2 Other means of identification

Product number -
Other names -

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:151985-13-6 SDS

151985-13-6Downstream Products

151985-13-6Relevant articles and documents

The Use of Two Linked Scanning Modes in Alternation to Analyse Metastable Peaks

Lacey, Michael J.,Macdonald, Colin G.

, p. 134 - 137 (1980)

Analyses of masses relative kinetic energies for metastable peaks may be achieved by the use in alternation of two types of linked scans of the electric sector voltage and magnetic field.The method is demonstrated by an appraisal of hydrogen exchange in molecular ions of 2-methyl-2H3>-benzoic acid.

Copper-Catalyzed Modular Access to N-Fused Polycyclic Indoles and 5-Aroyl-pyrrol-2-ones via Intramolecular N—H/C—H Annulation with Alkynes: Scope and Mechanism Probes

Liu, Yan-Hua,Song, Hong,Zhang, Chi,Liu, Yue-Jin,Shi, Bing-Feng

supporting information, p. 1545 - 1552 (2020/09/09)

Copper-catalyzed intramolecular N—H/C—H annulation with alkynes has been developed. A variety of densely functionalized heterocycles, such as pyrrolo[1,2-a]indoles, indolo[1,2-c]quinazolin-2-ones, oxazolo[3,4-a]indoles, and imidazo[1,5-a]indoles, were synthesized in an atom- and step-economical manner, owing to the high modularized feature of aniline moiety, the linker moiety, as well as the alkyne moiety. By simply changing the oxidant from di-tert-butyl peroxide (DTBP) to 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO), the reaction could readily be transformed to the aminooxygenation pathway, which grabs one oxygen atom from the TEMPO to generate 5-aroyl-pyrrol-2-ones. Mechanistic experiments indicate that vinyl radical is involved in this reaction and an amidyl-radical-initiated radical cascade might be responsible for this transformation.

Palladium catalyzed acetoxylation of benzylic C-H bonds using a bidentate picolinamide directing group

Cheng, Tao,Yin, Weiyu,Zhang, Yi,Zhang, Yingnan,Huang, Yong

supporting information, p. 1405 - 1411 (2014/03/21)

A general palladium catalyzed acetoxylation of benzylic C-H bonds has been developed. Picolinamides serve as an excellent directing group for the C-H activation of benzylic methyls. A wide range of 2-amino benzyl alcohol analogues were synthesized in good yields. The products demonstrated broad synthetic utilities toward various benzo-fused heterocycles. Mechanistic studies revealed the key rate-limiting C-H insertion step, which could be affected by the substitution pattern of the parent arene.

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