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40626-45-7

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40626-45-7 Usage

Appearance

White to light yellow crystalline solid

Solubility

Insoluble in water, soluble in most organic solvents

Odor

Strong and characteristic

Stability

Stable and non-reactive

Handling

Hazardous substance, can cause irritation to skin, eyes, and respiratory system

Safety Precautions

Work in well-ventilated area and wear appropriate protective equipment.

Check Digit Verification of cas no

The CAS Registry Mumber 40626-45-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,6,2 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40626-45:
(7*4)+(6*0)+(5*6)+(4*2)+(3*6)+(2*4)+(1*5)=97
97 % 10 = 7
So 40626-45-7 is a valid CAS Registry Number.

40626-45-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dichloro-2-phenylacetonitrile

1.2 Other means of identification

Product number -
Other names Dichlor-phenyl-acetonitril

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:40626-45-7 SDS

40626-45-7Relevant articles and documents

Novel synthesis method for oxophenylacetate

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Paragraph 0026; 0027; 0031; 0032; 0036; 0037; 0041; 0042, (2019/04/06)

The invention discloses a novel synthesis method for oxophenylacetate and belongs to the technical field of synthesis. The novel synthesis method comprises the steps: firstly, reacting benzonitrile and a halogenation reagent at 20-35 DEG C to obtain dihalogenated phenylacetonitrile; then, adding a mixed solution of acid and water into dihalogenated phenylacetonitrile at 35-55 DEG C, and carrying out a reaction at 50-60 DEG C for 2-8 h, wherein the molar ratio of a product I to the water to the acid is 1:(1-10):(1-10); and finally, adding alcohol into the reaction solution in the former step at50-60 DEG C, then, carrying out stirring, controlling the temperature at 60-70 DEG C, carrying out a constant-temperature reaction for 1-4 h, and carrying out cooling and extraction to obtain a target product. The reaction raw materials adopted in the method are wide in source and low in price, the operation process is simple, and the yield of the product is high.

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