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2-Octenoic acid, 5-hydroxy-, ethyl ester is a chemical compound with the molecular formula C10H18O3. It is an organic ester derived from 5-hydroxy-2-octenoic acid, where an ethyl group is attached to the hydroxyl group. 2-Octenoic acid, 5-hydroxy-, ethyl ester is characterized by a long-chain hydrocarbon with a double bond at the second carbon and a hydroxyl group at the fifth carbon. It is known for its potential applications in the synthesis of various chemical products and may be used in the fragrance and flavor industries due to its unique chemical structure. The compound's properties, such as its reactivity and solubility, can be influenced by the presence of the double bond and hydroxyl group, making it a versatile building block in organic chemistry.

6065-34-5

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6065-34-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6065-34-5 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 6065-34:
(6*6)+(5*0)+(4*6)+(3*5)+(2*3)+(1*4)=85
85 % 10 = 5
So 6065-34-5 is a valid CAS Registry Number.

6065-34-5SDS

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 5-hydroxyoct-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Octenoic acid,5-hydroxy-,ethyl ester

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:6065-34-5 SDS

6065-34-5Downstream Products

6065-34-5Relevant 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 (1984)

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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