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13295-96-0

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13295-96-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13295-96-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13295-96:
(7*1)+(6*3)+(5*2)+(4*9)+(3*5)+(2*9)+(1*6)=110
110 % 10 = 0
So 13295-96-0 is a valid CAS Registry Number.

13295-96-0SDS

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 p-tolylethynylpyridine

1.2 Other means of identification

Product number -
Other names 4-<4-Methyl-phenylethinyl>-pyridin

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:13295-96-0 SDS

13295-96-0Relevant articles and documents

Nickel-Catalyzed Sonogashira C(sp)-C(sp2) Coupling through Visible-Light Sensitization

Zhu, Da-Liang,Xu, Ruijie,Wu, Qi,Li, Hai-Yan,Lang, Jian-Ping,Li, Hong-Xi

, p. 9201 - 9212 (2020/08/14)

An efficient method for visible-light-initiated, nickel-catalyzed Sonogashira C(sp)-C(sp2) coupling has been developed via an energy-transfer mode. Thioxanthen-9-one as a photosensitizer could significantly accelerate the arylation of alkynes with a wide

Photo-dehydro-diels-alder reaction of 1-phenyl-2-(pyridyl)acetylenes in acidic aqueous solution

Zhuang, Junpeng,Zhang, Shuguang,Hao, Haijun,Jiang, Long

, p. 14 - 18 (2013/11/06)

The photocycloaddition of 1-(4-R-phenyl)-2-(4-pyridyl)acetylenes (R = H, Br, CH3, Cl) and 1-(4-Rphenyl)- 2-(2-pyridyl)acetylenes (R = H, Br, Cl) was carried out in acidic aqueous solution. The unexpected photo-dehydro-Diels-Alder reaction of these monomers was observed, and the results show that two monomers react in a head-to-tail manner and lead to the formation of 2-phenyl-1,3- di(pyridyl)naphthalene derivatives. This reaction presents a direct metal-free method to construct the 1,2,3-triaryl substituted naphthalenes from diarylacetylenes.

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