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88222-77-9

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88222-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88222-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,2,2 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88222-77:
(7*8)+(6*8)+(5*2)+(4*2)+(3*2)+(2*7)+(1*7)=149
149 % 10 = 9
So 88222-77-9 is a valid CAS Registry Number.

88222-77-9SDS

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 1-(4-Bromo-phenyl)-2-(2-methyl-5-phenyl-2,3-dihydro-[1,3,4]thiadiazol-2-yl)-ethanone

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).

More Details:88222-77-9 SDS

88222-77-9Relevant articles and documents

TAUTOMERISM IN THIOBENZOYLHYDRAZONES OF AROYLACETONES AND AROYLACETALDEHYDES

Yakimovich, S. I.,Zelenin, K. N.,Nikolaev, V. N.,Koshmina, N. V.,Alekseev, V. V.,Khrustalev, V. A.

, p. 1641 - 1646 (2007/10/02)

The products from the condensation of thiobenzohydrazide with aroylacetaldehydes in the crystalline state and in solutions have the structure of the corresponding Δ2-1,3,4-thiadiazolines.The products from the reaction of thiobenzohydrazide with aroylacetones in the condensed state are also the corresponding Δ2-1,3,4-thiadiazolines.In solutions in deuterochloroform they exist as mixtures of the thiadiazoline and 5-hydroxypyrazoline forms, and in solutions in DMSO-d6 a triple equilibrium is established which includes two ring forms and an open enehydrazine form.The introduction of electron-withdrawing substituents into the aromatic ring of the β-dicarbonyl component favors the enehydrazine and 5-hydroxypyrazoline tautomers.

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