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214072-10-3

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214072-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214072-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,0,7 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 214072-10:
(8*2)+(7*1)+(6*4)+(5*0)+(4*7)+(3*2)+(2*1)+(1*0)=83
83 % 10 = 3
So 214072-10-3 is a valid CAS Registry Number.

214072-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (5S)-2-Methoxy-1-[(benzyloxy)carbonyl]-5-methoxycarbonylpyrrolidine

1.2 Other means of identification

Product number -
Other names (2S)-1-benzyl 2-methyl 5-methoxypyrrolidine-1,2-dicarboxylate

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:214072-10-3 SDS

214072-10-3Relevant articles and documents

BETA-HYDROXY HETEROCYCLIC AMINES AND THEIR USE IN THE TREATMENT OF HYPERGLYCAEMIA

-

, (2019/04/11)

There is herein provided a compound of formula (I) or a pharmaceutically acceptable salt thereof, wherein X, R1, ring A, m and n have meanings as provided in the description.

Synthesis of indolizidines (-)-195B, (-)-223AB and (-)-239AB: (2S,5R)- l-[(benzyloxy)carbonyl]-2-methoxycarbonyl-5-(4pentenyl)pyrrolidine as a versatile chiral building block

Celimene, Catherine,Dhimane, Hamid,Lhommet, Gerard

, p. 10457 - 10468 (2007/10/03)

The total syntheses of three levogyre 3,5-disubstituted indolizidines, (-)-195B, (-)-223AB and (-)-239AB are described. The employed strategy is based on the utilization of the common enantiopure trans 2,5-disubstituted pyrrolidine 3, which is assembled b

A short and highly stereocontrolled total synthesis of (3R,5R,8aR)-3-n-Butyl-5-methylindolizidine

Celimene, Catherine,Dhimane, Hamid,Le Bail, Marc,Lhommet, Gerard

, p. 6105 - 6106 (2007/10/02)

Total synthesis of (-) (3R,5R,8aR)-3-n-Butyl-5-methylindolizidine is described in 9 steps (22% overall yield) from L-proline.

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