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90794-46-0

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90794-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90794-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,9 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90794-46:
(7*9)+(6*0)+(5*7)+(4*9)+(3*4)+(2*4)+(1*6)=160
160 % 10 = 0
So 90794-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11Cl/c1-8(2)7-9-5-3-4-6-10(9)11/h3-6H,1,7H2,2H3

90794-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-2-(2-methylprop-2-enyl)benzene

1.2 Other means of identification

Product number -
Other names 2-(2-Methylprop-2-en-1-yl)chlorobenzene

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:90794-46-0 SDS

90794-46-0Relevant articles and documents

Cross-coupling synthesis of methylallyl alkenes: Scope extension and mechanistic study

Tabélé, Clémence,Curti, Christophe,Kabri, Youssef,Primas, Nicolas,Vanelle, Patrice

, p. 22890 - 22899 (2016/01/25)

Cross-coupling reactions between 2-methyl-2-propen-1-ol and various boronic acids are used to obtain aromatic-(2-methylallyl) derivatives. However, deboronation or isomerization side reactions may occur for several boronic acids. We describe herein the synthesis of original alkenes with good yields under mild reaction conditions that decrease these side reactions. The scope of this environmentally benign reaction is thereby extended to a wide variety of boronic acids. A mechanistic study was conducted and suggested a plausible catalytic cycle mechanism, pointing to the importance of the Lewis acidity of the boronic acid used.

Tandem Cyclization-Cycloaddition Reaction of Rhodium Carbenoids. Studies Dealing with Intramolecular Cycloadditions

Padwa, Albert,Hornbuckle, Susan F.,Fryxell, Glen E.,Zhang, Zhijia J.

, p. 5747 - 5757 (2007/10/02)

A series of 5-alkenyl-1-diazo-2,5-pentanediones, when treated with a catalytic quantity of rhodium(II) acetate, were found to give cycloadducts derived from the intramolecular trapping of a carbonyl ylide intermediate.Tethers of three or four methylenes r

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