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67452-27-1

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67452-27-1 Usage

Chemical Properties

cis-4-Decenyl acetate has a pleasant, oily and rosy odor. This compound is also reported to possess spicy, floral aroma.

Occurrence

Reportedly present in grapefruit juice (Citrus paradesi).

Check Digit Verification of cas no

The CAS Registry Mumber 67452-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,4,5 and 2 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 67452-27:
(7*6)+(6*7)+(5*4)+(4*5)+(3*2)+(2*2)+(1*7)=141
141 % 10 = 1
So 67452-27-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H22O2/c1-3-4-5-6-7-8-9-10-11-14-12(2)13/h7-8H,3-6,9-11H2,1-2H3/b8-7-

67452-27-1SDS

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 dec-4-enyl acetate

1.2 Other means of identification

Product number -
Other names CIS-4-DECEN-1-YL ACETATE

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:67452-27-1 SDS

67452-27-1Upstream product

67452-27-1Downstream Products

67452-27-1Relevant articles and documents

Stereospecific conversion of iodohydrin derivatives into alkenes by means of an allylsilane-titanium tetrachloride system and its application to steseoretentive deoxygenation of epoxides

Yachi, Kentaro,Maeda, Katsuya,Shinokubo, Hiroshi,Oshima, Koichiro

, p. 5161 - 5164 (2007/10/03)

Whereas erythro-iodohydrin derivatives provided (E)-alkenes with high stereoselectivity upon treatment with titanium tetrachloride in the presence of allyltrimethylsilane, the corresponding threo isomers afforded (Z)-alkenes exclusively. The reaction was applied to the stereoretentive conversion of epoxides to alkenes.

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