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1-Methyl-3-cyclohexen-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33061-16-4

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33061-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33061-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,6 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 33061-16:
(7*3)+(6*3)+(5*0)+(4*6)+(3*1)+(2*1)+(1*6)=74
74 % 10 = 4
So 33061-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O/c1-7(8)5-3-2-4-6-7/h2-3,8H,4-6H2,1H3

33061-16-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methylcyclohex-3-en-1-ol

1.2 Other means of identification

Product number -
Other names 4-Hydroxi-4-methyl-cyclohexen

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:33061-16-4 SDS

33061-16-4Downstream Products

33061-16-4Relevant academic research and scientific papers

Mechanism of the 1,3-sigmatropic shift of 2-vinylcyclobutanol alkoxides

Harris, Nathan J.,Gajewski, Joseph J.

, p. 6121 - 6129 (2007/10/02)

The rate of rearrangement of 2-vinylcyclobutanol was studied in dimethyl sulfoxide and tetrahydrofuran solvents. Rearrangement to 3-cyclohexenol in 1% aqueous DMSO is catalyzed by lithium hydroxide. When lithium bromide is added to this medium, the rate i

SYNTHESIS OF Z-ALLYLIC ACETATES VIA FRAGMENTATION OF CYCLIC HOMOALLYLIC ALCOHOLS

Ramaiah, P.,Rao, A. S.

, p. 2119 - 2120 (2007/10/02)

Z-Allylic acetates (6a-6e) having an additional functional group as ketone or aldehyde were prepared via the fragmentation of the homoallylic alcohols (5a-5e) in the presence of lead tetraacetate.

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