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3H-Pyrrolo[1,2-a]azepin-3-one, octahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111633-57-9

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111633-57-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111633-57-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,6,3 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 111633-57:
(8*1)+(7*1)+(6*1)+(5*6)+(4*3)+(3*3)+(2*5)+(1*7)=89
89 % 10 = 9
So 111633-57-9 is a valid CAS Registry Number.

111633-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,5,6,7,8,9,9a-octahydropyrrolo[1,2-a]azepin-3-one

1.2 Other means of identification

Product number -
Other names 3H-Pyrrolo[1,2-a]azepin-3-one,octahydro

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:111633-57-9 SDS

111633-57-9Upstream product

111633-57-9Downstream Products

111633-57-9Relevant academic research and scientific papers

Bicyclization of aza-compounds by positive halide ions. II. Lactams and some related cyclizations

Elofson, Richard M.,Gadallah, Fahmi F.,Laidler, James K.

, p. 2770 - 2773 (2007/10/02)

Anodic oxidation of lactams in the presence of halide ions produced excellent yields of bicyclic compounds with reactants having rings in the range of eight to ten atoms (C7 to C9).Smaller rings did not react to form bicyclic products and larger rings gave reduced yields.Attempts were made to cyclize non-cyclic amides and to bicyclize cycloheptyl and cyclooctyl acetamide with limited success.

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