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7515-16-4

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7515-16-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7515-16-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7515-16:
(6*7)+(5*5)+(4*1)+(3*5)+(2*1)+(1*6)=94
94 % 10 = 4
So 7515-16-4 is a valid CAS Registry Number.

7515-16-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 3-(4-methylphenyl)prop-2-ynoate

1.2 Other means of identification

Product number -
Other names methyl p-methylphenylpropiolate

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:7515-16-4 SDS

7515-16-4Relevant articles and documents

Catalytic tricarbonylation of alkynes with palladium catalysts

Izawa, Yusuke,Shimizu, Isao,Yamamoto, Akio

, p. 1060 - 1061 (2005)

A novel catalytic process of introducing three CO units into alkynes by palladium-catalyzed alkoxycarbonylation was developed. Based on the fundamental studies on the behavior of organopalladium complexes, mechanisms to account for the mono- and tricarbon

Au(I) Catalyzed Synthesis of Densely Substituted Pyrazolines and Dihydropyridines via Sequential Aza-Enyne Metathesis/6π-Electrocyclization

Sugimoto, Kenji,Kosuge, Shuto,Sugita, Takae,Miura, Yuka,Tsuge, Kiyoshi,Matsuya, Yuji

supporting information, p. 3981 - 3985 (2021/05/26)

A gold(I) autotandem catalysis protocol is reported for the de novo synthesis of densely substituted pyrazolines and dihydropyridines from the corresponding imine derivatives in a highly regioselective fashion via a one-pot aza-enyne metathesis/6π-electrocyclization sequence. The substituents on the nitrogen atom of the imine perfectly control the reaction pathways from the pivotal 1-azabutadiene intermediate; thus, carbazates were converted into pyrazolines via 6π-electrocyclization of α,β-unsaturated hydrazones, while aryl imines provided dihydropyridines via 6π-electrocyclization of 3-azahexatrienes.

Oxidant- and additive-free simple synthesis of 1,1,2-triiodostyrenes by one-pot decaroboxylative iodination of propiolic acids

Ghosh, Subhankar,Ghosh, Rajat,Chattopadhyay, Shital K.

supporting information, (2020/09/15)

A metal- and oxidant-free facile synthesis of a range of 1,1,2-triiodostryrene derivatives has been developed which utilizes a simple decarboxylative triiodination of propiolic acids using molecular iodine and sodium acetate in a one-pot manner. Electron-

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