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Carbamic acid, [1-(azidomethyl)-4-oxobutyl](phenylmethyl)-, phenylmethyl ester, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132256-84-9

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132256-84-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132256-84-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,5 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132256-84:
(8*1)+(7*3)+(6*2)+(5*2)+(4*5)+(3*6)+(2*8)+(1*4)=109
109 % 10 = 9
So 132256-84-9 is a valid CAS Registry Number.

132256-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-4-<N-benzyl-N-(benzyloxycarbonyl)amino>-5-azido-pentanal

1.2 Other means of identification

Product number -
Other names (S)-4-[N-benzyl-N-(benzyloxycarbonyl)amino]-5-azido-pentanal

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:132256-84-9 SDS

132256-84-9Relevant academic research and scientific papers

Synthesis of (-)-Slaframine and Related Indolizidines

Pearson, William H.,Bergmeier, Stephen C.,Williams, John P.

, p. 3977 - 3987 (2007/10/02)

An enantioselective synthesis of the indolizidine alkaloid (-)-slaframine 1 is reported.Reductive double cyclization of the azido epoxy tosylate 48 afforded the indolizidine 52, which was converted to (-)-slaframine in two steps.The cyclization substrate

A Synthesis of (-)-Slaframine and (-)-1,8a-Diepislaframine

Pearson, William H.,Bergmeier, Stephen C.

, p. 1976 - 1978 (2007/10/02)

Reductive cyclization of the optically pure azido epoxides 12 and 13 afforded the indolizidines 14 and 16, which were converted into (-)-slaframine 1 and (-)-1,8a-diepislaframine 18.

Synthesis of indolidines by the 1,3-dipolar cycloaddition of azides with methylenecyclopropanes followed by cyclopropyumine rearrangement

Heidt, Philip C.,Bergmeier, Stephen C.,Pearson, William H.

, p. 5441 - 5444 (2007/10/02)

Cyclic imines 6a and 6b were obtained by the intramolecular 1,3-dipolar cycloaddition of azides with methylenecyclopropanes. Acid catalyzed rearrangement produced bicyclic (-)-enamines 7, which upon reduction provided indoilizidenes 8. A similar strategy was used for the synthesis of (-)-8a-epi-desacctoxyslaframine 16.

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