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18492-65-4

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18492-65-4 Usage

Description

CIS-4-HEPTENAL DIETHYL ACETAL is a chemical compound known for its distinct taste and aroma characteristics. It is often used in the flavor and fragrance industry due to its unique properties.

Uses

Used in Flavor Industry:
CIS-4-HEPTENAL DIETHYL ACETAL is used as a flavoring agent for its green, dairy-like, creamy, apple, vegetable, and strawberry taste characteristics at a concentration of 20 ppm.
Used in Fragrance Industry:
CIS-4-HEPTENAL DIETHYL ACETAL is used as a fragrance ingredient for its ability to impart a green, creamy, and fruity scent to various products.

Check Digit Verification of cas no

The CAS Registry Mumber 18492-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,9 and 2 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18492-65:
(7*1)+(6*8)+(5*4)+(4*9)+(3*2)+(2*6)+(1*5)=134
134 % 10 = 4
So 18492-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O2/c1-4-7-8-9-10-11(12-5-2)13-6-3/h7-8,11H,4-6,9-10H2,1-3H3/b8-7+

18492-65-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,7-diethoxyhept-3-ene

1.2 Other means of identification

Product number -
Other names cis-4-HEPTENAL DIETHYL ACETAL

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:18492-65-4 SDS

18492-65-4Relevant articles and documents

A CHEMOSELECTIVE DESULFURIZATION METHOD VIA HOMOGENEOUS NICKEL CATALYSIS

Trost, Barry M.,Ornstein, Paul L.

, p. 3463 - 3466 (2007/10/02)

Isopropylmagnesium bromide in the presence of bis-(triphenylphosphino)-nickel(II) chloride reduces vinyl sulfides stereospecifically to the corresponding olefins without overreduction - a process which serves as a key step in the synthesis of the sex pheromone of the Douglas fir tussock moth.

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