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1,3-Cyclohexadiene, 1-methoxy-4-methyl- is an organic compound with the molecular formula C8H12O. It is a derivative of cyclohexadiene, featuring a methyl group at the 4-position and a methoxy group at the 1-position. This chemical is characterized by its conjugated diene system, which contributes to its chemical reactivity and potential applications in organic synthesis. The compound is a colorless liquid with a distinct aroma and is insoluble in water but soluble in organic solvents. It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity, it is important to handle 1,3-Cyclohexadiene, 1-methoxy-4-methyl- with care, following proper safety protocols.

2161-94-6

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2161-94-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2161-94-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2161-94:
(6*2)+(5*1)+(4*6)+(3*1)+(2*9)+(1*4)=66
66 % 10 = 6
So 2161-94-6 is a valid CAS Registry Number.

2161-94-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-4-methylcyclohexa-1,3-diene

1.2 Other means of identification

Product number -
Other names 4-methyl-1-methoxy-1,3-cyclohexadiene

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:2161-94-6 SDS

2161-94-6Relevant academic research and scientific papers

HIV PROTEASE INHIBITORS

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, (2008/06/13)

Peptide mimics, having a constrained peptide backbone conformation, are HIV protease inhibitors. A compound of this invention is, for example, 3-Benzyl-5(alaninyl-1-aminoethyl)-2,3,6,7-tetrahydro-N-azepinyl-2-propionyl-valinyl-valinyl methyl ester.

Synthesis Based on Cyclohexadienes. V. A New Approach to the Synthesis of A-Ring Aromatic Steroids: a Formal Total Synthesis of (+/-)-Estrone

Rao, G. S. R. Subba,Banerjee, D. K.,Devi, L. Uma,Sheriff, Uma

, p. 187 - 203 (2007/10/02)

A new strategy for the construction of A-ring aromatic steroids which resulted in the formal total synthesis of estrone is described.Thus reaction of the adduct (9), obtained from 1-methoxy-4-methylcyclohexa-1,4-diene and acrolein, with 3-(m-methoxyphenyl

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