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114251-21-7

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  • 2,5-Cyclohexadien-1-ol, 4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-4-methoxy-1-methyl-, cis-

    Cas No: 114251-21-7

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114251-21-7 Usage

Structure

Contains a cyclohexadiene ring with a hydroxy, methoxy, and methyl group attached
Contains a tert-butyldimethylsilyloxy (TBS) group attached to the cyclohexadiene ring

Isomer

cis isomer

Usage

Commonly used in organic synthesis and as a reagent in various chemical reactions

Purpose

Its properties and reactivity make it useful for the creation of new organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 114251-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,5 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 114251-21:
(8*1)+(7*1)+(6*4)+(5*2)+(4*5)+(3*1)+(2*2)+(1*1)=77
77 % 10 = 7
So 114251-21-7 is a valid CAS Registry Number.

114251-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-((tert-butyldimethylsilyl)oxy)-4-methoxy-1-methylcyclohexa-2,5-dienol

1.2 Other means of identification

Product number -
Other names -

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:114251-21-7 SDS

114251-21-7Relevant articles and documents

The Addition of Organolithium Reagents to Quinone Silyl Methyl Monoketals. A Useful Expedient in the Synthesis of p-Quinols Having Acid-Sensitive Groups

Stern, Alan J.,Swenton, John S.

, p. 2465 - 2468 (2007/10/02)

Acid hydrolyses of dimethyl ketals 4-alkyl- and 4-aryl-4-hydroxy-2,5-cyclohexadienones having an acid-sensitive functionality often afford low or no yields of the respective 4-substituted 4-hydroxy-2,5-cyclohexadienones (p-quinols).However, addition of me

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