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445-69-2

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445-69-2 Usage

Physical state

Colorless liquid

Odor

Strong, pungent

Main use

Production of high-performance polymers (e.g., Kevlar, Teflon)

Reactivity

Highly reactive

Hazardous reactions

Can react violently with water, alcohols, and amines

Potential hazards

Potentially hazardous if not handled properly

Carcinogenicity

Considered a potential carcinogen

Handling precautions

Should be handled with extreme caution in a controlled laboratory setting

Check Digit Verification of cas no

The CAS Registry Mumber 445-69-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 5 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 445-69:
(5*4)+(4*4)+(3*5)+(2*6)+(1*9)=72
72 % 10 = 2
So 445-69-2 is a valid CAS Registry Number.

445-69-2SDS

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 benzene-1,2-dicarbonyl fluoride

1.2 Other means of identification

Product number -
Other names o-Phthaloylfluorid

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:445-69-2 SDS

445-69-2Relevant articles and documents

Gram-Scale Preparation of Acyl Fluorides and Their Reactions with Hindered Nucleophiles

Barbasiewicz, Micha?,Tryniszewski, Micha?

, (2021/11/30)

A series of acyl fluorides was synthesized at 100 mmol scale using phase-transfer-catalyzed halogen exchange between acyl chlorides and aqueous bifluoride solution. The convenient procedure consists of vigorous stirring of the biphasic mixture at room temperature, followed by extraction and distillation. Isolated acyl fluorides (usually 7-20 g) display excellent purity and can be transformed into sterically hindered amides and esters when treated with lithium amide bases and alkoxides under mild conditions.

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