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Proline, 3,3-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

204267-20-9

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204267-20-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204267-20-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,2,6 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 204267-20:
(8*2)+(7*0)+(6*4)+(5*2)+(4*6)+(3*7)+(2*2)+(1*0)=99
99 % 10 = 9
So 204267-20-9 is a valid CAS Registry Number.

204267-20-9SDS

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 (2S)-3,3-dimethylpyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Proline,3,3-dimethyl

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:204267-20-9 SDS

204267-20-9Downstream Products

204267-20-9Relevant academic research and scientific papers

Benzyl 2-cyano-3,3-dimethyl-1-pyrrolidinecarboxylate, a versatile intermediate for the synthesis of 3,3-dimethylproline derivatives

Medina, Jesus R.,Blackledge, Charles W.,Erhard, Karl F.,Axten, Jeffrey M.,Miller, William H.

, p. 3946 - 3949 (2008/09/19)

(Chemical Equation Presented) The synthesis of racemic nitrile (±)-9 was accomplished in four steps and 58% overall yield from the known pyrrolidinone 5. Nitrile (±)-9 was resolved via preparative chiral HPLC to afford optically pure nitriles (+)-9 and (-

Thrombin inhibitors

-

, (2008/06/13)

Compounds of the invention are useful in inhibiting thrombin and associated thrombotic occlusions having the following structure: or a pharmaceutically acceptable salt thereof, e.g. where R3 is —CH2NH2, —CH2CH2NH2, or —CH2NHC(O)OC(CH3)3.

Histidine derivatives

-

, (2008/06/13)

Compounds of the formula STR1 wherein R, R1, R2, R3 and R4 represent certain specified substituent groups. The compounds exhibit activity in the reserpine induced hypothermia test.

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