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4-methylhex-5-enal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

68235-57-4

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68235-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68235-57-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,2,3 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 68235-57:
(7*6)+(6*8)+(5*2)+(4*3)+(3*5)+(2*5)+(1*7)=144
144 % 10 = 4
So 68235-57-4 is a valid CAS Registry Number.

68235-57-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylhex-5-enal

1.2 Other means of identification

Product number -
Other names 4-methyl-5-hexen-1-al

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:68235-57-4 SDS

68235-57-4Upstream product

68235-57-4Downstream Products

68235-57-4Relevant academic research and scientific papers

Diene compound and process for producing the same

-

, (2008/06/13)

The invention provides a chain diene compound with desirable regioselectivity, in the presence of a specific ruthenium compound. This chain diene compound is a promising raw material for terpene. It has a structure represented by the general formula (IX): wherein R1represents H, a C1-C6alkyl group which may be substituted or a C2-C6alkenyl group which may be substituted, R2represents a phenyl group which may have a C1-C4alkyl group or a C1-C12acyloxy group which may have a phenyl group or a naphthyl group, or a benzyl group or R2is a hydroxy group which reversibly forms an aldehyde group through shifting of the position of the double bond adjacent to said hydroxy group. The chain diene compound is produced by reacting 2-substituted-1,3-butadienes with terminal olefins in the presence of a ruthenium compound in a hydrophilic solvent. Further, the above method provides an inexpensive process for preparing a mild fragrant component and a perfume composition, such as 4-methyl-5-hexen-1-al and 4-vinyl-8-methyl-7-nonenal.

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