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benzyl 2-({[tert-butyl(dimethyl)silyl]oxy}methyl)piperidine-1-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1072344-35-4

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1072344-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1072344-35-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,2,3,4 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1072344-35:
(9*1)+(8*0)+(7*7)+(6*2)+(5*3)+(4*4)+(3*4)+(2*3)+(1*5)=124
124 % 10 = 4
So 1072344-35-4 is a valid CAS Registry Number.

1072344-35-4SDS

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 benzyl 2-({[tert-butyl(dimethyl)silyl]oxy}methyl)piperidine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:1072344-35-4 SDS

1072344-35-4Relevant academic research and scientific papers

Catalytic kinetic resolution of cyclic secondary amines

Binanzer, Michael,Hsieh, Sheng-Ying,Bode, Jeffrey W.

supporting information; experimental part, p. 19698 - 19701 (2012/01/13)

The catalytic resolution of racemic cyclic amines has been achieved by an enantioselective amidation reaction featuring an achiral N-heterocyclic carbene catalyst and a new chiral hydroxamic acid cocatalyst working in concert. The reactions proceed at room temperature, do not generate nonvolatile byproducts, and provide enantioenriched amines by aqueous extraction.

NEW BRADYKININ B1 ANTAGONISTS

-

, (2008/12/08)

The invention relates to compounds of formula (I), wherein R1 to R5 and X1 to X4, n and m have the meaning as cited in the description and the claims. Said compounds are useful as Bradykinin B1 antagonists. The

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