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13706-68-8

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13706-68-8 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 68, p. 2108, 1946 DOI: 10.1021/ja01214a510

Check Digit Verification of cas no

The CAS Registry Mumber 13706-68-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,0 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13706-68:
(7*1)+(6*3)+(5*7)+(4*0)+(3*6)+(2*6)+(1*8)=98
98 % 10 = 8
So 13706-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2/c11-7-6-10(8-12)9-4-2-1-3-5-9/h1-5,10H,6H2/t10-/m1/s1

13706-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenylbutanedinitrile

1.2 Other means of identification

Product number -
Other names 2-phenyl-succinonitrile

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:13706-68-8 SDS

13706-68-8Relevant articles and documents

-

Mowry

, p. 2108 (1946)

-

Tetraarylphosphonium inner-salts (TAPIS) as both Lewis base catalyst and phase tag

Guo, Shuhui,Mi, Xueling

supporting information, p. 2881 - 2884 (2017/07/11)

Tetraarylphosphonium inner-salts (TAPIS) have been designed, synthesized and verified as recyclable and reusable Lewis base catalysts. The resulted TAPIS catalyst has been successfully applied in Michael addition, cyanation and trifluoromethylation reactions.

The reactivity of TMSN3 with ruthenium cyclopropenyl complexes containing different ligands and different substituent at Cγ

Sung, Hui-Ling,Hsu, Hsiu-Ling

experimental part, p. 1280 - 1288 (2011/04/25)

Ruthenium vinylidene complexes 2a-2c containing indenyl and bidentate dppe ligands can be obtained in efficient yields. Treatment of the cationic ruthenium vinylidene complexes with n-Bu4NOH in acetone yields the neutral cyclopropenyl products (η5-C9H7)(dppe)Ru- CC(Ph)CHR (3) (3a, R = Ph; 3b, R = CN; 3c, R = p-C6H4-CN) via the deprotonation reaction. Reaction of complexes 3a and 3c with Me 3SiN3 (TMSN3) the N-coordinated complexes 4a and 4c can be obtained as stable products. Complex 3b containing CN group at Cγ in the cyclopropenyl ring reacts with TMSN3 yielded the tetrazolate complex 5b. Similar cyclopropenyl products containing indenyl and two triphenylphosphine ligands 3′ can also be synthesized. Reaction of complex 3b′ with TMSN3 also yielded the tetrazolate complex as the major product. And the minor products are [Ru]-N3 and organic compound 6b. Reaction of 3a′ and 3c′ with TMSN3 yielded [Ru]-N3. The corresponding organic products can also be obtained via the N3- attacking the metal center in the N-coordinated complexes 4a′ and 4c′.

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