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2-Butenoic acid, 4-(1-hydroxycyclohexyl)-, (E)-, also known as 4-(1-hydroxycyclohexyl)but-2-enoic acid, is an organic compound with the molecular formula C10H16O3. It is a derivative of butenoic acid, featuring a cyclohexyl group with a hydroxyl group attached to the first carbon and a double bond between the second and third carbons of the butenoic acid chain. 2-Butenoic acid, 4-(1-hydroxycyclohexyl)-, (E)- is characterized by its unique structure, which combines the properties of a carboxylic acid with a cyclohexane ring and a double bond, making it a versatile building block in organic synthesis. It is used in the production of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its ability to form esters and other derivatives with different functional groups.

7465-10-3

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7465-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7465-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7465-10:
(6*7)+(5*4)+(4*6)+(3*5)+(2*1)+(1*0)=103
103 % 10 = 3
So 7465-10-3 is a valid CAS Registry Number.

7465-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name γ-(1-Hydroxy-1-cyclohexyl)-crotonsaeure

1.2 Other means of identification

Product number -
Other names trans-4-(1-Hydroxy-cyclohexyl)-but-2-ensaeure

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:7465-10-3 SDS

7465-10-3Relevant academic research and scientific papers

SUR LA REACTION DE PREFORMATSKY. PREPARATION ET REACTIVITE DE L'ORGANOZINCIQUE ISSU DU SEL BROMOZINCIQUE DE L'ACIDE γ-BROMOCROTONIQUE

Bellassoued, M.,Habbachi, F.,Gaudemar, M.

, p. 1299 - 1306 (1985)

The condensation of aldehydes and ketones with the bromozinc salt derived from γ-bromocrotonic acid, in the presence of zinc, yield to the "linear" and "branched" unsaturated hydroxyacids.These latters, which represent the kinetic products of the reaction, equilibrate at the alcoholate state to give, after hydrolysis, the "linear" compounds.

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