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64187-83-3

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64187-83-3 Usage

Chemical Properties

Clear, colorless liquid; green, wine-like aroma.

Occurrence

Reported as a component of Mastic leaf oil at 0.07%

Aroma threshold values

Medium strength odor, tropical type; recommend smelling in a 10.00% solution or less.

Check Digit Verification of cas no

The CAS Registry Mumber 64187-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,8 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 64187-83:
(7*6)+(6*4)+(5*1)+(4*8)+(3*7)+(2*8)+(1*3)=143
143 % 10 = 3
So 64187-83-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-3-5-6-7-8(9)10-4-2/h5-6H,3-4,7H2,1-2H3/b6-5-

64187-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (Z)-hex-3-enoate

1.2 Other means of identification

Product number -
Other names Ethyl (Z)hex-3-enoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:64187-83-3 SDS

64187-83-3Downstream Products

64187-83-3Relevant articles and documents

Silica-supported dendrimer-palladium complex-catalyzed selective hydrogenation of dienes to monoolefins

Zweni, Pumza P.,Alper, Howard

, p. 725 - 731 (2007/10/03)

The selective hydrogenation of cyclic and acyclic dienes to monoolefins occurs under very mild conditions, in the presence of silica-supported PAMAM-Pd complexes. The activity and selectivity of this reaction is sensitive to the dendrimer structure. These dendritic complexes display excellent recycle properties, retaining activity for up to eight recycles.

A Note on Stereochemical Observation of the Deprotonation of Ethyl-2-Alkenoates

Krebs, Ernst-Peter

, p. 1023 - 1025 (2007/10/02)

Deprotonation of ethyl (E)-2-alkenoates 1, 3 and 4 yields after protonation the double bond migrated (3 Z)-isomers 5, 7 and 9 as major products.In contrast, deprotonation and reprotonation of ethyl (Z)-2-pentanoate (2) gives the (3 E)-isomer 6 exclusively

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