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Cyclohexanone, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80684-13-5

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80684-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80684-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,8 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 80684-13:
(7*8)+(6*0)+(5*6)+(4*8)+(3*4)+(2*1)+(1*3)=135
135 % 10 = 5
So 80684-13-5 is a valid CAS Registry Number.

80684-13-5SDS

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 3-[tert-butyl(dimethyl)silyl]oxycyclohexan-1-one

1.2 Other means of identification

Product number -
Other names 3-t-butyldimethylsiloxycyclohexanone

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:80684-13-5 SDS

80684-13-5Downstream Products

80684-13-5Relevant academic research and scientific papers

Cascade radical carbonylations leading to 3-substituted cyclohexanones

Uenoyama, Yoshitaka,Fukuyama, Takahide,Ryu, Ilhyong

, p. 2342 - 2344 (2007/10/03)

Tin radical mediated [5+1]-annulation methods leading to 3-substituted cyclohexanones were investigated. Cyclohexanones having a quaternary center at the 3-position were synthesized in good yields by allyltin-mediated three- and four-component cascade rea

Oxidation of Olefins into α-Phenylseleno Carbonyl Compounds. Highly Regioselective anti-Markownikoff Type Oxidation of Allylic Alcohol Derivatives

Shimizu, Makoto,Takeda, Ryo,Kuwajima, Isao

, p. 3510 - 3517 (2007/10/02)

By using (C6H5Se)2-t-BuOOH or (C6H5Se)(2-) (C6H5SeO)2O system, oxoselenylation reaction of C=C bonds have been examined with allylic and homoallylic alcohol derivatives, and substituted cyclohexenes, and allyl t-butyldimethylsilyl ethers are found to unde

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