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ACETANILIDE-4'-D1 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16625-79-9

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16625-79-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16625-79-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16625-79:
(7*1)+(6*6)+(5*6)+(4*2)+(3*5)+(2*7)+(1*9)=119
119 % 10 = 9
So 16625-79-9 is a valid CAS Registry Number.

16625-79-9SDS

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 ACETANILIDE-4'-D1

1.2 Other means of identification

Product number -
Other names 4-Deutero-acetanilid

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:16625-79-9 SDS

16625-79-9Downstream Products

16625-79-9Relevant academic research and scientific papers

Continuous-flow catalytic deuterodehalogenation carried out in propylene carbonate

Orsy, Gy?rgy,Fül?p, Ferenc,Mándity, István M.

, p. 956 - 961 (2019)

A selective continuous-flow (CF) deuterodehalogenation approach is described performed in propylene carbonate, which is considered as one of the greenest solvents. Various CF technologies are known for hydrodehalogenation reactions; however, they are not

Copper-catalysed low-temperature water-gas shift reaction for selective deuteration of aryl halides

Bartling, Stephan,Beller, Matthias,Bourriquen, Florian,Junge, Kathrin,Li, Wu,Liu, Weiping,Qu, Ruiyang,Rockstroh, Nils

, p. 14033 - 14038 (2021/11/12)

The introduction of deuterium atoms into organic compounds is of importance for basic chemistry, material sciences, and the development of drugs in the pharmaceutical industry, specifically for identification and quantification of metabolites. Hence, methodologies for the synthesis of selectively labelled compounds continue to be a major area of interest for many scientists. Herein, we present a practical and stable heterogeneous copper catalyst, which permits for dehalogenative deuterationviawater-gas shift reaction at comparably low temperature. This novel approach allows deuteration of diverse (hetero)aryl halides with good functional group tolerance, and no reduction of the aromatic rings or other easily reducible formyl and cyano groups. Multi-gram experiments show the potential of this method in organic synthesis and medicinal chemistry.

A convenient method for palladium-catalyzed reductive deuteration of organic substrates using deuterated hypophosphite in D2O

Oba, Makoto

, p. 215 - 219 (2015/05/20)

A convenient method for the deuteration of organic substrates using deuterated hypophosphite as the deuterium source was investigated. Transfer deuteration of organic substrates, such as aromatic halides, alkenes, alkynes, epoxides, and O-benzyl derivativ

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