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3-Ethynylhept-1-en-3-ol, also known as 3-ethynyl-1-hepten-3-ol, is an organic compound with the molecular formula C9H14O. It is a colorless liquid with a distinct, floral odor. This chemical is characterized by the presence of an ethynyl (acetylene) group and a double bond in its structure, which contributes to its unique properties. It is used in the synthesis of various fragrances and flavors, particularly in the production of natural-like scents and tastes. The compound is also of interest in the field of organic chemistry for its potential applications in the creation of more complex molecules. Due to its reactivity, it is important to handle 3-ethynylhept-1-en-3-ol with care, following proper safety protocols.

6929-27-7

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6929-27-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6929-27-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6929-27:
(6*6)+(5*9)+(4*2)+(3*9)+(2*2)+(1*7)=127
127 % 10 = 7
So 6929-27-7 is a valid CAS Registry Number.

6929-27-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethynylhept-1-en-3-ol

1.2 Other means of identification

Product number -
Other names 1-HEPTEN-3-OL,3-ETHYNYL

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:6929-27-7 SDS

6929-27-7Relevant academic research and scientific papers

Enantioselective Inverse Electron Demand (3 + 2) Cycloaddition of Palladium-Oxyallyl Enabled by a Hydrogen-Bond-Donating Ligand

Zheng, Yin,Qin, Tianzhu,Zi, Weiwei

, p. 1038 - 1045 (2021/01/25)

Cycloaddition reactions between oxyallyl cations and alkenes are important transformations for the construction of ring systems. Although (4 + 3) cycloaddition reactions of oxyallyl cations are well-developed, (3 + 2) cycloadditions remain rare, and an as

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