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3-Cyclohexene-1-methanol,a-methyl-
Cas No: 17264-01-6
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10 Gram
500 Kilogram/Month
Zibo Hangyu Biotechnology Development Co., Ltd
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3-Cyclohexene-1-methanol,a-methyl-
Cas No: 17264-01-6
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Antimex Chemical Limied
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1-cyclohex-2-en-1-ylethanol
Cas No: 17264-01-6
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BOC Sciences
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17264-01-6 Usage

Properties

Unsaturated alcohol with a methyl group and a hydroxyl group attached to a cyclohexene ring

Common Uses

Production of flavors, fragrances, and pharmaceuticals

Industrial Application

Valuable intermediate in organic synthesis

Biological and Pharmacological Studies

Potential biological and pharmacological activities

Potential Applications

Medicine and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 17264-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,6 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 17264-01:
(7*1)+(6*7)+(5*2)+(4*6)+(3*4)+(2*0)+(1*1)=96
96 % 10 = 6
So 17264-01-6 is a valid CAS Registry Number.

17264-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	1-cyclohex-2-en-1-ylethanol

1.2 Other means of identification

Product number	-
Other names	Methanol,methyl-3-cyclohexenyl

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:17264-01-6 SDS

17264-01-6Upstream product

17264-01-6Downstream Products

17264-01-6Relevant articles and documents

Lithium Borohydride-catalysed Selective Reduction of Carbonyl Group of Conjugated and Unconjugated Alkenones with Borane in Tetrahydrofuran

Arase, Akira,Hoshi, Masayuki,Yamaki, Tuneharu,Nakanishi, Hirohumi

, p. 855 - 856 (1994)

In the presence of a catalytic amount of LiBH4, BH3 in THF selectively reduced the carbonyl group of conjugated and unconjugated alkenones at -50 deg C to quantitatively provide the corresponding alkenols on subsequent hydrolysis.

Hydroxymercuration of Nonconjugated Dienes in Aqueous Micelles

Link, Cynthia M.,Jansen, David K.,Sukenik, Chaim N.

, p. 7798 - 7799 (1980)

Formal hydration of non-activated terminal olefins using tandem catalysts

Yang, Yongsheng,Guo, Jiayi,Ng, Huimin,Chen, Zhiyong,Teo, Peili

supporting information, p. 2608 - 2611 (2014/03/21)

The hydration of terminal olefins to secondary alcohols has been achieved using a Pd(ii)/Ru(ii) catalyst combination with high regioselectivity and yields. Both vinyl arenes and aliphatic olefins can be hydrated easily with the tandem catalyst system using a low catalyst loading of 1 mol%. The Royal Society of Chemistry 2014.

Synthesis and attractiveness for Ceratitis capitata Wied. Males of Δ3cyclohexenylalkylcarbinol acetates. IV (1)

Guiotto,Manzini,Pastorini,Rodighiero

, p. 441 - 446 (2007/10/02)

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CAS

17264-01-6