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5-(HydroxyMethyl)cyclohex-2-enol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156041-33-7

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156041-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156041-33-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,0,4 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 156041-33:
(8*1)+(7*5)+(6*6)+(5*0)+(4*4)+(3*1)+(2*3)+(1*3)=107
107 % 10 = 7
So 156041-33-7 is a valid CAS Registry Number.

156041-33-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxymethylcyclohex-2-en-1-ol

1.2 Other means of identification

Product number -
Other names 5-hydroxymethyl-cyclohex-2-enol

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:156041-33-7 SDS

156041-33-7Relevant academic research and scientific papers

An Approach to the Synthesis of Stenine

Zhu, Liang,Lauchli, Ryan,Loo, Mandy,Shea, Kenneth J.

, p. 2269 - 2271 (2008/02/05)

A type 2 N-acylnitroso intramolecular Diels-Alder reaction followed by reductive N - O bond cleavage formed the B and C rings of the Stemona alkaloid stenine. Further elaboration provided the functionalized tricyclic core.

Anionic Cycloaddition with Thiophthalides: an Integrated Approach to the Synthesis of Olivin and Pillaromycinone

Majumdar, Gita,Pal, Ranjan,Murty, Kadiyala V. S. N.,Mal, Dipakranjan

, p. 309 - 316 (2007/10/02)

A systematic study of the potential reactivity of the thiophthalides 4 and 18 - 20 as 1,4-dipolar synthons, has shown that 3-phenylthiothiophthalide 19 is the best annulating agent for the preparation of tricyclic intermediates related to olivin.The reagent 19 underwent anionic cycloaddition with cyclohex-2-enone 5a in the presence of lithium tert-butoxide to give the anthracenones 24a and 25 in a combined yield of 90percent.

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