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Silane, (1,1-dimethylethyl)dimethyl[[(1R)-2-methyl-2-cyclopenten-1-yl]oxy]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

777076-74-1

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777076-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 777076-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,7,0,7 and 6 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 777076-74:
(8*7)+(7*7)+(6*7)+(5*0)+(4*7)+(3*6)+(2*7)+(1*4)=211
211 % 10 = 1
So 777076-74-1 is a valid CAS Registry Number.

777076-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl-dimethyl-[(1R)-2-methylcyclopent-2-en-1-yl]oxysilane

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:777076-74-1 SDS

777076-74-1Relevant academic research and scientific papers

Rendering schrock-type molybdenum alkylidene complexes air stable: User-friendly precatalysts for alkene metathesis

Heppekausen, Johannes,Fuerstner, Alois

supporting information; experimental part, p. 7829 - 7832 (2011/10/05)

A matter of convenience: Schrock molybdenum alkylidenes are amongst the most powerful olefin metathesis catalysts known to date, but their sensitivity to air and moisture mandates their handling in a glove-box or by Schlenk techniques. This inconvenience is circumvented by using the corresponding phenanthroline- or bipyridine adducts, which are bench-stable and hence very user-friendly. The active species can be liberated from these precatalysts in uncompromised form on treatment with ZnCl2 in toluene (see scheme).

Stereoselective synthesis of the lituarine tricyclic spiroacetal

Robertson, Jeremy,Meo, Paul,Dallimore, Jonathan W. P.,Doyle, Bryan M.,Hoarau, Christophe

, p. 3861 - 3863 (2007/10/03)

(Chemical Equation Presented) Oxidative cyclizations of 2-(4-hydroxybutyl)furan derivatives provide spirobutenolide acetals directly; on the basis of this methodology, we describe an asymmetric synthesis of a tricyclic spirobutenolide precursor to the C(7

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