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1-(2,2-Diphenyl-vinyl)-2,2,3,3-tetracyan-cyclobutan is a complex organic compound characterized by its unique molecular structure. It features a cyclobutan ring with four cyano groups (-CN) attached to the carbon atoms at positions 2, 2, 3, and 3. Additionally, a 2,2-diphenyl-vinyl group is attached to the 1-position of the cyclobutan ring, which consists of a vinyl group (C=C) bonded to two phenyl rings. 1-(2,2-Diphenyl-vinyl)-2,2,3,3-tetracyan-cyclobutan is known for its rigid structure and potential applications in various chemical and material science fields, such as the synthesis of advanced polymers and the development of new materials with unique properties.

5171-94-8

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5171-94-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5171-94-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5171-94:
(6*5)+(5*1)+(4*7)+(3*1)+(2*9)+(1*4)=88
88 % 10 = 8
So 5171-94-8 is a valid CAS Registry Number.

5171-94-8SDS

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 6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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

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More Details:5171-94-8 SDS

5171-94-8Relevant academic research and scientific papers

Reaktion von trans-1-Arylbutadienen und 1,1-Diarylbutadienen mit Tetracyanethylen (TCNE) und 2,2-Bis(trifluormethyl)ethylen-1,1-dicarbonitril (BTF): Kinetische Studie

Drexler, J.,Lindermayer, R.,Hassan, M. A.,Sauer, J.

, p. 2559 - 2562 (2007/10/02)

Kinetic data (substituent effects, solvent effects, activation parameter) are reported for the reactions of trans-1-arylbutadienes 1 and 1,1-diarylbutadienes 3 with TCNE 4 and BTF 5. (2+2)- and (4+2)-cycloadducts 7 respectively 9 can rearrange or undergo cycloreversions with quite different reaction rates depending on the substituent in the aryl-ring.

Reaktion von trans-1-Arylbutadienen und 1,1-Diarylbutadienen mit Tetracyanethylen (TCNE) und 2,2-Bis(trifluormethyl)ethylen-1,1-dicarbonitril (BTF) : Praeparative Studie.

Drexler, J.,Lindermayer, R.,Hassan, M. A.,Sauer, J.

, p. 2555 - 2558 (2007/10/02)

Trans-1-Arylbutadienes 5 yield normal DIELS-ALDER-adducts 9 and 10 with TCNE 7 and BTF 8.On the other hand 1,1-diarylbutadienes 6 reacting with the same dienophiles give 1:1-adducts 12/13 and/or 14, respectively substitution products 11.At higher temperat

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