Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, 1-(2-butenyl)-2-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20983-15-7

Post Buying Request

20983-15-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

20983-15-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20983-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,9,8 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20983-15:
(7*2)+(6*0)+(5*9)+(4*8)+(3*3)+(2*1)+(1*5)=107
107 % 10 = 7
So 20983-15-7 is a valid CAS Registry Number.

20983-15-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-but-2-enyl-2-methylbenzene

1.2 Other means of identification

Product number -
Other names o-crotyltoluene

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:20983-15-7 SDS

20983-15-7Downstream Products

20983-15-7Relevant academic research and scientific papers

Electrophilic allylation of arenes with in situ generated allyltriarylbismuthonium compound: The Bismuth-mediated polarity inversion of allylsilanes

Matano, Yoshihiro,Yoshimune, Masanori,Suzuki, Hitomi

, p. 7475 - 7478 (2007/10/02)

Reaction of triarylbismuth difluorides 1 with allyltrimethylsilane 2 in CH2Cl2 in the presence of BF3·OEt2 at low temperature generates allyltriarylbismuthonium compound 3 as a pale yellow solution, in which aromatic hydrocarbons and ethers, triphenylphosphine, dimethyl sulfide, p-toluenesulfinate, and thiophenol are all readily allylated to afford the corresponding allyl derivatives in moderate to good yields.

REACTION OF 1,3-ALKADIENES WITH ARENEDIAZONIUM CHLORIDES IN THE PRESENCE OF IRON(II) CHLORIDE

Ganushchak, N. I.,Obushak, N. D.,Polishchuk, O. P.

, p. 633 - 639 (2007/10/02)

The reaction of arenediazonium chlorides with 1,3-alkadienes in the presence of iron(II) chloride was investigated.It was established that the reaction takes place with the formation of products from chloroarylation of the dienes, telomerization, and additive dimerization.A method is proposed for the synthesis of diaryloctatetraenes containing substituents in the aromatic rings and in the aliphatic chain.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 20983-15-7