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Benzene, 1,2-bis[(1Z)-2-bromoethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183181-22-8

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183181-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183181-22-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,1,8 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 183181-22:
(8*1)+(7*8)+(6*3)+(5*1)+(4*8)+(3*1)+(2*2)+(1*2)=128
128 % 10 = 8
So 183181-22-8 is a valid CAS Registry Number.

183181-22-8SDS

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 (Z,Z)-o-bis(β-bromovinyl)benzene

1.2 Other means of identification

Product number -
Other names (Z,Z)-o-bis(β-bromovinyl)benzene

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:183181-22-8 SDS

183181-22-8Relevant academic research and scientific papers

A versatile route to 3-benzoheteroepines containing group 15 and 16 heavier elements involving several novel ring systems, and their thermal stabilities.

Yasuike, Shuji,Kiharada, Tsutomu,Tsuchiya, Takashi,Kurita, Jyoji

, p. 1283 - 1288 (2003)

The C-unsubstituted 3-benzoheteroepines (2a-g) containing group 15 (P, As, Sb, and Bi) and group 16 (S, Se, and Te) heavier elements were prepared by the reaction of the corresponding metal reagents with (Z,Z)-o-bis(beta-lithiovinyl)benzene (5) which was derived in two steps from a common o-phthalaldehyde (3). The heteroepines (2) thus obtained were thermally labile towards heteroatom extrusion, and their half-lives on heating estimated from (1)H-NMR spectral analysis showed that the 3-benzoheteroepines (2) were far less stable than the corresponding 1-benzoheteroepines (1). The 2,4-bis(trimethylsilyl)-3-benzoheteroepines (17) containing Sb, Bi, and Te were also prepared from o-diiodobenzene (9) in 6 steps and were found to be more stable than the corresponding C-unsubstituted heteroepines (2).

Synthesis and thermal stability of 3-substituted 3-benzostibepines

Yasuike, Shuji,Ikoma, Masaaki,Kakusawa, Naoki,Tsuchiya, Takashi,Kurita, Jyoji

, p. 659 - 667 (2009)

Fully unsaturated 3-benzostibepines having various aryl groups on antimony have been prepared by a ring closure reaction of an appropriate antimony dihalide (ArSbBr2) with (Z,Z)-1,2-bis(2-lithiovinyl)benzene generated by treatment of (Z,Z)-1,2-

A versatile synthesis of the group 15 and 16 3-benzoheteroepines involving the first isolated examples of several C-unsubstituted 3-benzoheteroepines

Yasuike, Shuji,Kiharada, Tsutomu,Kurita, Jyoji,Tsuchiya, Takashi

, p. 2183 - 2184 (2007/10/03)

Group 15 (P, As, Sb and Bi) and group 16 (S, Se and Te) 3-benzoheteroepines 2, involving the first isolated examples of several C-unsubstituted fully unsaturated 3-benzoheteroepines, are prepared in two steps from (Z,Z)-o-bis(β-bromovinyl)benzene 4 and their thermal stabilities examined.

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