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80814-98-8

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80814-98-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80814-98-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,8,1 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80814-98:
(7*8)+(6*0)+(5*8)+(4*1)+(3*4)+(2*9)+(1*8)=138
138 % 10 = 8
So 80814-98-8 is a valid CAS Registry Number.

80814-98-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name diethyl 4-phenylbuta-1,3-dien-2-yl phosphate

1.2 Other means of identification

Product number -
Other names Phosphoric acid,diethyl 1-methylene-3-phenyl-2-propenyl ester

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:80814-98-8 SDS

80814-98-8Relevant articles and documents

Iron-Catalyzed Tertiary Alkylation of Terminal Alkynes with 1,3-Diesters via a Functionalized Alkyl Radical

Tian, Ming-Qing,Shen, Zhen-Yao,Zhao, Xuefei,Walsh, Patrick J.,Hu, Xu-Hong

supporting information, p. 9706 - 9711 (2021/03/19)

Direct oxidative C(sp)?H/C(sp3)?H cross-coupling offers an ideal and environmentally benign protocol for C(sp)?C(sp3) bond formations. As such, reactivity and site-selectivity with respect to C(sp3)?H bond cleavage have remained a persistent challenge. Herein is reported a simple method for iron-catalyzed/silver-mediated tertiary alkylation of terminal alkynes with readily available and versatile 1,3-dicarbonyl compounds. The reaction is suitable for an array of substrates and proceeds in a highly selective manner even employing alkanes containing other tertiary, benzylic, and C(sp3)?H bonds alpha to heteroatoms. Elaboration of the products enables the synthesis of a series of versatile building blocks. Control experiments implicate the in situ generation of a tertiary carbon-centered radical species.

Cross-Coupling of Enol Phosphates with Trimethylsilylmethylmagnesium Halides Catalyzed by Nickel or Palladium Complexes; A Selective Synthesis of Allylsilanes

Hayashi, Tamio,Fujiwa, Takaaki,Okamoto, Yasuo,Katsuro, Yoshio,Kumada, Makoto

, p. 1001 - 1003 (2007/10/02)

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