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77422-30-1

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77422-30-1 Usage

Chemical class

Pyrrolidine class of compounds

Type of compound

Cyclic secondary amine derivative

Structural feature

Methyl group attached to the first carbon atom of the pyrrolidine ring

Isotope presence

Contains three deuterium atoms (heavy isotopes of hydrogen)

Prefix notation

"1-methyl" for the methyl group attachment, "D3" for the three deuterium atoms

Applications

Organic synthesis and pharmaceutical research

Significance

Important for studying the properties and behavior of pyrrolidine derivatives

Check Digit Verification of cas no

The CAS Registry Mumber 77422-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,2 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77422-30:
(7*7)+(6*7)+(5*4)+(4*2)+(3*2)+(2*3)+(1*0)=131
131 % 10 = 1
So 77422-30-1 is a valid CAS Registry Number.

77422-30-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(trideuteriomethyl)pyrrolidine

1.2 Other means of identification

Product number -
Other names N-Methyl-d3-pyrrolidine

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:77422-30-1 SDS

77422-30-1Downstream Products

77422-30-1Relevant articles and documents

Mass Spectrometry of Organic Compounds of The Group V Elements VI-A New Type of Amine Fragmentation Under Electron Impact

Kostyanovsky, R.G.,Voznesensky, V. N.,Kadorkina, G. K.,El'natanov, Yu. I.

, p. 412 - 418 (2007/10/02)

A new type of amine fragmentations under electron impact is elucidated for proline, sarcosine and aspartic acid derivatives and aminomethylphosphines of the general formula R2NCH2X.Ordinary α-cleavage affording the R2N+=CH2 ion is suppressed by elimination of a neutral HX particle and + ion formation, or M-HX neutral particle ejection and generation of an + ion from +.Such fragmentation is ensured by the presence of an α-heteroatom (N, O, P, S) in one substituent (X) and CO2R type delocalizing group in the α-position of the other substituent (R2N).

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