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Check Digit Verification of cas no

The CAS Registry Mumber 80989-82-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,8 and 9 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 80989-82:
(7*8)+(6*0)+(5*9)+(4*8)+(3*9)+(2*8)+(1*2)=178
178 % 10 = 8
So 80989-82-8 is a valid CAS Registry Number.

80989-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name	diethyl 2-hydroxy-2-(2-oxo-2-phenylethyl)malonate

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

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

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80989-82-8Relevant articles and documents

Electrocatalytic Activation of Donor–Acceptor Cyclopropanes and Cyclobutanes: An Alternative C(sp3)?C(sp3) Cleavage Mode

Brandt, Felix,Jacob, Christoph R.,Jones, Peter G.,Kolb, Simon,Petzold, Martin,Werz, Daniel B.

supporting information, p. 15928 - 15934 (2021/06/21)

We describe the first electrochemical activation of D–A cyclopropanes and D–A cyclobutanes leading after C(sp3)?C(sp3) cleavage to the formation of highly reactive radical cations. This concept is utilized to formally insert molecula

Molecular Design by Cycloaddition Reaction. Part 43. Cycloaddition Reactions of Silyl Enol Ethers of 2-Acetylfuran and -thiophene and Related Benzo Analogues

Sasaki, Tadashi,Ishibashi, Yukio,Ohno, Masatomi

, p. 1972 - 1997 (2007/10/02)

The title compounds (5, 6, 11, 12 and 13) underwent cycloaddition reactions with typical dienophiles followed by oxidative rearomatization.The reactions of (5) and (6) with heterodienophiles gave rather open-chain adducts via a zwitterionic interm

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80989-82-8