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1901-34-4

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1901-34-4 Usage

General Description

2,4-Cycloheptadien-1-one is a chemical compound known for its strong aroma and yellow color. It is used in the production of fragrances, as well as in organic synthesis and chemical research. The compound is highly reactive due to the presence of an alpha, beta-unsaturated ketone group, and is susceptible to nucleophilic addition reactions. It is also a key intermediate in the synthesis of various pharmaceuticals and other organic molecules. The compound is sensitive to light and air, and should be stored in a cool, dark place to prevent degradation.

Check Digit Verification of cas no

The CAS Registry Mumber 1901-34-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1901-34:
(6*1)+(5*9)+(4*0)+(3*1)+(2*3)+(1*4)=64
64 % 10 = 4
So 1901-34-4 is a valid CAS Registry Number.

1901-34-4SDS

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 cyclohepta-2,4-dien-1-one

1.2 Other means of identification

Product number -
Other names Cycloheptadienone

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:1901-34-4 SDS

1901-34-4Relevant articles and documents

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Hine,K.E.,Childs,R.F.

, p. 144 - 145 (1972)

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Synthetic studies on the ingenane diterpenes. An improved entry into a trans-intrabridgehead system.

Rigby, James H,Bazin, Berangere,Meyer, J Hoyt,Mohammadi, Farahnaz

, p. 799 - 801 (2007/10/03)

[reaction: see text] The efficient construction of an ingenol intermediate exhibiting insideminus signoutside intrabridgehead stereochemistry is reported. The sequence features the net conversion of a cis-intrabridgehead compound into a highly strained trans-species via palladium-mediated isomerization of an allylic epoxide followed by a low-temperature alkoxide-accelerated 1,5-hydrogen migration.

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