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Bicyclo[4.1.0]heptane-7-carboxylic acid, 1-[[dimethyl[2,4,6-tris(1,1-dimethylethyl)phenoxy]silyl]oxy]-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

90288-94-1

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90288-94-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90288-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,8 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90288-94:
(7*9)+(6*0)+(5*2)+(4*8)+(3*8)+(2*9)+(1*4)=151
151 % 10 = 1
So 90288-94-1 is a valid CAS Registry Number.

90288-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (1α)-1-((2,4,6-Tri-tert-butylphenoxy)(dimethyl)siloxy)bicyclo(4.1.0)-heptan-7-carbonsaeure-methylester

1.2 Other means of identification

Product number -
Other names (1α)-1-[(2,4,6-Tri-tert-butylphenoxy)(dimethyl)siloxy]bicyclo[4.1.0]-heptan-7-carbonsaeure-methylester

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:90288-94-1 SDS

90288-94-1Relevant academic research and scientific papers

Synthesis of 2-Siloxy-substituted Methyl Cyclopropanecarboxylates

Kunkel, Elisabeth,Reichelt, Ingrid,Reissig, Hans-Ulrich

, p. 512 - 530 (2007/10/02)

2-Siloxy-substituted methyl cyclopropanecarboxylates C - useful building blocks in synthesis - are obtained in great variety and with good yields from the silyl enol ethers E and methyl diazoacetate (D) under copper salt catalysis.Whereas the regiochemical and stereochemical properties of E are completely transferred to the cyclopropanes C, the stereoselectivity concerning the position of the methoxycarbonyl group is low.The 1H and 13C data used to determine the configurations of compounds C are discussed.

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