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7-Azabicyclo[4.1.0]heptane, 7-(4-bromobenzoyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108577-15-7

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108577-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108577-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,5,7 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 108577-15:
(8*1)+(7*0)+(6*8)+(5*5)+(4*7)+(3*7)+(2*1)+(1*5)=137
137 % 10 = 7
So 108577-15-7 is a valid CAS Registry Number.

108577-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-azabicyclo[4.1.0]heptan-7-yl-(4-bromophenyl)methanone

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:108577-15-7 SDS

108577-15-7Relevant academic research and scientific papers

Synthesis of N-acylaziridines from β-amido selenides

Ward,Cooper,Ward

, p. 944 - 945 (2007/10/03)

The low temperature oxidation of β-amido selenides with MCPBA affords the corresponding β-amido selenones. In situ treatment of the selenones with KOtBu gives N-acylaziridines in good to excellent yield.

The synthesis of N-benzoyl aziridines from β-benzamidoalkyl phenyl selenides

Ward, Virginia R.,Cooper, Matthew A.,Ward, A. David

, p. 195 - 201 (2007/10/03)

β-Benzamidoalkyl phenyl selenides can be oxidised, using mCPBA, to the corresponding selenones which can be cyclised to oxazolines or aziridines depending on the reaction conditions. In neutral or weakly basic conditions the oxazoline is the major product

Antiarrhythmic use of aminocycloalkylamides

-

, (2008/06/13)

Benzamides, benzeneacetamides, and spirocyclobenzamides and -benzeneacetamides of the formula which were previously disclosed as having analgesic utility been found to have antiarrhythmic utility.

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