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2,5-Cyclohexadiene-1-carboxylic acid, 1-(3-chloropropyl)-3,5-dimethyl-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111112-92-6

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111112-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111112-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,1,1 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 111112-92:
(8*1)+(7*1)+(6*1)+(5*1)+(4*1)+(3*2)+(2*9)+(1*2)=56
56 % 10 = 6
So 111112-92-6 is a valid CAS Registry Number.

111112-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3-chloropropyl)-3-(methoxycarbonyl)-1,5-dimethyl-1,4-cyclohexadiene

1.2 Other means of identification

Product number -
Other names 3-carbometoxy-3-(3-chloropropyl)-1,5-dimethyl-1,4-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:111112-92-6 SDS

111112-92-6Relevant academic research and scientific papers

Intramolecular Cycloadditions to Oxyallyl Zwitterions Generated from Photorearrangements of 2,5-Cyclohexadien-1-ones

Schultz, Arthur G.,Macielag, Mark,Plummer, Mark

, p. 391 - 395 (2007/10/02)

Photorearrangement of 2,5-cyclohexadien-1-one 9a gave phenols 12 and 13, while 9b gave bicyclohexenone 10b.No evidence for the formation of an azide-zwitterion cycloadduct was obtained from these examples.However, the 3,6-dimethoxy analogue 9c provided the bridged triazene 14, for which X-ray crystallographic studies confirmed structural assignments for 14 and previously obtained triazenes 5a and 5b. 4--3-methoxy-4-(nethoxycarbonyl)cyclohexa-2,5-dien-1-one (17) photorearranged to bicyclohexenone 18 and phenol 19.The 4-acetoxymethyl derivatives 20a and 20b gave the bridged furan adducts 23a, and 23b in excellent yield.Acetoxymethyl-substituted triazene 27 was obtained from 26c; 27 slowly gave alcohol 28 on exposure to the atmosphere.

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