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336-13-0

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336-13-0 Usage

General Description

1-Bromoundecafluorocyclohexane is a chemical compound that belongs to the class of perfluorinated compounds. It is a highly fluorinated organic compound that is used in various industrial applications, including as a solvent, refrigerant, and propellant. It is also used as a component in the production of polymers and plastics. The compound is known for its high chemical stability, low reactivity, and resistance to heat and chemicals. However, it is also a persistent organic pollutant that can bioaccumulate in the environment and pose risks to human health and the ecosystem. As a result, its use is regulated and restricted in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 336-13-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,3 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 336-13:
(5*3)+(4*3)+(3*6)+(2*1)+(1*3)=50
50 % 10 = 0
So 336-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C6BrF11/c7-1(8)2(9,10)4(13,14)6(17,18)5(15,16)3(1,11)12

336-13-0SDS

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-Bromoundecafluorocyclohexane

1.2 Other means of identification

Product number -
Other names 1-bromo-1,2,2,3,3,4,4,5,5,6,6-undecafluorocyclohexane

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:336-13-0 SDS

336-13-0Downstream Products

336-13-0Relevant articles and documents

-

Brice,Simmons

, p. 4016 (1951)

-

REACTION OF POLYFLUORINATED CYCLOALKANES WITH VANADIUM, ANTIMONY, AND NIOBIUM PENTAFLUORIDES

Bardin, V. V.,Avramenko, A. A.,Petrov, V. A.,Krasil'nikov, V. A.,Karelin, A. I.,et al

, p. 536 - 540 (2007/10/02)

Polyfluorinated cycloalkanes are fluorinated by vanadium pentafluoride at 25-60 deg C.Conjugation between the C=C bond of the cycloalkene and the aromatic ring facilitates the reaction, whereas the reactivity of the unconjugated olefin fragment is lower than or is equal to that of the aromatic ring.The antimony pentafluoride fluorinates polyhalogenocyclohexenes at 150 deg C, while niobium pentafluoride does not exhibit fluorinating characteristics under these conditions.

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