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5364-22-7

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5364-22-7 Usage

Molecular Weight

254.64 g/mol

Physical State

Solid

Appearance

Off-white to pale yellow crystalline solid

Solubility

Slightly soluble in water, soluble in organic solvents like ethanol, dichloromethane, and acetone

Reactivity

Highly reactive due to the presence of the acyl chloride functional group

Uses

Organic synthesis, pharmaceutical production, agrochemicals, fine chemicals, and dyes preparation

Functional Group

Acyl chloride

Natural Occurrence

Derived from isatin, a naturally occurring compound found in plants and fruits

Preparation

Key building block in the preparation of a wide range of pharmaceuticals and agrochemicals

Reagent

Used as a reagent in synthetic chemistry to introduce the acyl group onto other molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 5364-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5364-22:
(6*5)+(5*3)+(4*6)+(3*4)+(2*2)+(1*2)=87
87 % 10 = 7
So 5364-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H14Cl3FN2O/c1-10-5-4-6-11(9-10)14(23)22-15(16(17,18)19)21-13-8-3-2-7-12(13)20/h2-9,15,21H,1H3,(H,22,23)

5364-22-7SDS

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 3-methyl-N-[2,2,2-trichloro-1-(2-fluoroanilino)ethyl]benzamide

1.2 Other means of identification

Product number -
Other names L-2-methyl-2-(phthalimido)acetyl chlorid

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:5364-22-7 SDS

5364-22-7Relevant articles and documents

SULFUR YLIDES. 3. SYNTHESIS OF KETO-GROUP STABILIZED AMINO-CONTAINING SULFUR YLIDES FROM AMINO ACIDS

Tolstikov, G. A.,Galin, F. Z.,Lakeev, S. N.,Khalilov, L. M.,Sultanova, V. S.

, p. 535 - 541 (2007/10/02)

An effective path of synthesis was developed of new synthetic intermediates, the optically active, keto-group stabilized amino-substituted sulfur ylides.

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