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1120-70-3

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1120-70-3 Usage

General Description

1,1-Difluorocyclopentane is a colorless liquid organic compound with the chemical formula C5H8F2. It is a fluorinated cycloalkane that is commonly used as a refrigerant and propellant in aerosol products. With a boiling point of -35.4°C, it has low toxicity and is not highly flammable, making it a relatively safe option for use in various applications. Its stable molecular structure and low reactivity make it an attractive compound for use as a solvent, and it is also used in the manufacture of pharmaceuticals and agrochemicals. Additionally, it has potential as a potential energy source due to its high energy density. Despite its usefulness, 1,1-difluorocyclopentane is a potent greenhouse gas and is being phased out in many applications due to its contribution to climate change.

Check Digit Verification of cas no

The CAS Registry Mumber 1120-70-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1120-70:
(6*1)+(5*1)+(4*2)+(3*0)+(2*7)+(1*0)=33
33 % 10 = 3
So 1120-70-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H8F2/c6-5(7)3-1-2-4-5/h1-4H2

1120-70-3SDS

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 1,1-DIFLUOROCYCLOPENTANE

1.2 Other means of identification

Product number -
Other names gem-difluorocyclopentane

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:1120-70-3 SDS

1120-70-3Upstream product

1120-70-3Relevant articles and documents

FLUORIERUNGSEIGENSCHAFTEN VON WF6

Haas, A.,Maciej, Th.

, p. 581 - 588 (1982)

WF6 reacts with aliphatic carbonyl- or carboxyl derivates to form the corresponding difluorides or carbonic acid fluorides.Fluorination of carbonyl compounds makes the presence of a Lewis acid like BF3 necessary.Trifluoromethyl compounds are not available in this way.Selective fluorination of alcoholes with WF6 is not possible.

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