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2311-13-9

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2311-13-9 Usage

Composition

One bromine atom and one fluorine atom

Physical State

Colorless, flammable gas

Odor

Faint, sweet

Common Uses

Refrigerant, production of pharmaceuticals, agrochemicals, and other organic compounds

Additional Applications

Solvent for cleaning and degreasing

Toxicity

Moderately toxic (risk to human health and environment if mishandled)

Check Digit Verification of cas no

The CAS Registry Mumber 2311-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,1 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2311-13:
(6*2)+(5*3)+(4*1)+(3*1)+(2*1)+(1*3)=39
39 % 10 = 9
So 2311-13-9 is a valid CAS Registry Number.
InChI:InChI=1/C2H4BrF/c1-2(3)4/h2H,1H3

2311-13-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-1-FLUOROETHANE

1.2 Other means of identification

Product number -
Other names 1-Brom-1-fluorethan

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:2311-13-9 SDS

2311-13-9Upstream product

2311-13-9Relevant articles and documents

-

Fields,R. et al.

, p. 1370 - 1375 (1970)

-

FLP-Catalyzed Monoselective C-F Functionalization in Polyfluorocarbons at Geminal or Distal Sites

Gupta, Richa,Mandal, Dipendu,Jaiswal, Amit K.,Young, Rowan D.

supporting information, p. 1915 - 1920 (2021/04/05)

We report frustrated Lewis pair (FLP)-catalyzed monoselective C-F activation in a range of aliphatic polyfluorocarbons with equivalent geminal and distal C-F positions. This methodology can be applied to aromatic-, ether-, thioether-, and alkyl-supported fluoromethyl groups. We expand the range of FLP base partners that work with monoselective C-F activation to include sulfide. The activated products can be subsequently functionalized via SN2 substitutions, photoredox-alkylations, and Suzuki couplings.

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