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Ethyl 2-ethenyl-3-hydroxyhexanoate is a chemical compound with the molecular formula C10H18O3. It is an ester derived from 2-ethenyl-3-hydroxyhexanoic acid and ethanol. This organic compound is characterized by the presence of a double bond (C=C) in the 2-position, a hydroxyl group (-OH) in the 3-position, and an ester group (-COO-) connecting the carboxylic acid and the ethanol. It is a colorless liquid with a fruity, floral odor and is used in the fragrance industry as a flavoring agent and a component in perfumes. The compound is also known for its potential applications in the synthesis of various chemicals and materials due to its unique structure.

6065-35-6

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6065-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6065-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,6 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6065-35:
(6*6)+(5*0)+(4*6)+(3*5)+(2*3)+(1*5)=86
86 % 10 = 6
So 6065-35-6 is a valid CAS Registry Number.

6065-35-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-ethenyl-3-hydroxyhexanoate

1.2 Other means of identification

Product number -
Other names opt.inakt.-3-Hydroxy-2-vinyl-hexansaeure-ethylester

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:6065-35-6 SDS

6065-35-6Downstream Products

6065-35-6Relevant academic research and scientific papers

Regioselectivity in the Reformatsky Reaction of 4-Bromocrotonate. Role of the Catalyst and the Solvent in the Normal vs. Abnormal Modes of Addition to Carbonyl Substrates

Rice, Leonard E.,Boston, M.Craig,Finklea, Harry O.,Suder, Billy Jo,Frazier, James O.,Hudlicky, Tomas

, p. 1845 - 1848 (2007/10/02)

The regioselectivity of addition of the organozinc reagent derived from ethyl 4-bromocrotonate to 10 carbonyl substrates was found to be dependent on the polarity of solvents and the hardness of metal catalysts.

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