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Benzene, 1-(cyclopropylidenemethyl)-4-(1,1-dimethylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

918831-65-9

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918831-65-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 918831-65-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,8,8,3 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 918831-65:
(8*9)+(7*1)+(6*8)+(5*8)+(4*3)+(3*1)+(2*6)+(1*5)=199
199 % 10 = 9
So 918831-65-9 is a valid CAS Registry Number.

918831-65-9SDS

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 1-tert-butyl-4-(cyclopropylidenemethyl)benzene

1.2 Other means of identification

Product number -
Other names Benzene,1-(cyclopropylidenemethyl)-4-(1,1-dimethylethyl)

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:918831-65-9 SDS

918831-65-9Relevant academic research and scientific papers

Nickel-Catalyzed Favorskii-Type Rearrangement of Cyclobutanone Oxime Esters to Cyclopropanecarbonitriles

Fang, Ping,Mei, Tian-Sheng,Shuai, Bin

supporting information, p. 1637 - 1641 (2021/10/02)

A nickel-catalyzed base-promoted rearrangement of cyclobutanone oxime esters to cyclopropanecarbonitriles was developed. The ring opening of cyclobutanone oxime esters occurs at the sterically less hindered side. A base-promoted nickelacyclobutane intermediate, formed in situ, is assumed to be involved in the formation of the product.

Rhodium-Catalyzed Ring-Opening Hydroacylation of Alkylidenecyclopropanes with Chelating Aldehydes for the Synthesis of γ,δ-Unsaturated Ketones

Li, Hong-Shuang,Lu, Shi-Chao,Chang, Zhi-Xin,Hao, Liqiang,Li, Fu-Rong,Xia, Chengcai

supporting information, p. 5145 - 5150 (2020/07/04)

The first intermolecular ring-opening hydroacylation of alkylidenecyclopropanes with chelating aldehydes through a rhodium-catalyzed acrylamide-promoted protocol is reported. This highly efficient catalytic system enables the direct synthesis of a diverse

A new protocol for nickel-catalysed regio- and stereoselective hydrocyanation of allenes

Arai, Shigeru,Hori, Hiroto,Amako, Yuka,Nishida, Atsushi

supporting information, p. 7493 - 7496 (2015/05/04)

Regio- and stereoselective hydrocyanation under nickel catalysis is described. This report shows that allenyl C-C double bonds are discriminated and converted to the corresponding carbonitriles as a single product. The key functionalities for achieving high regio- and stereocontrol are aryl and cyclopropyl groups in the substrates. This journal is

Enantioselective synthesis of γ-aryl-γ-butyrolactones by sequential asymmetric epoxidation, ring expansion, and Baeyer-Villiger oxidation

Wang, Bin,Shen, Yu-Mei,Shi, Yian

, p. 9519 - 9521 (2007/10/03)

(Chemical Equation Presented) This paper describes an enantioselective synthesis of γ-butyrolactones, using the N-tolyl-substituted oxazolidinone-containing ketone as catalyst and Oxone as oxidant via a sequential asymmetric epoxidation of benzylidenecyclopropanes, ring expansion, and Baeyer-Villiger oxidation. Up to 91% ee was obtained. Optically active cyclobutanones can also be obtained by suppressing the Baeyer-Villiger oxidation with use of more ketone catalyst and less Oxone.

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