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1,3-Butadiene, 1,1-difluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

590-91-0

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590-91-0 Usage

Physical state at room temperature

Colorless gas

Primary uses

Production of elastomers, plastics, and synthetic rubbers

Hazardous classification

Hazardous air pollutant

Health risks

Carcinogenic to humans (potentially causing cancer in those exposed to high levels over extended periods)

Regulatory measures

Strict regulations on manufacture, use, and disposal to protect human health and the environment

Check Digit Verification of cas no

The CAS Registry Mumber 590-91-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 590-91:
(5*5)+(4*9)+(3*0)+(2*9)+(1*1)=80
80 % 10 = 0
So 590-91-0 is a valid CAS Registry Number.

590-91-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-difluorobuta-1,3-diene

1.2 Other means of identification

Product number -
Other names 1,1-difluorobutadiene

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:590-91-0 SDS

590-91-0Downstream Products

590-91-0Relevant academic research and scientific papers

KINETICS AND MECHANISM OF THE SYNTHESIS OF DIFLUOROBENZENES BY THERMAL REACTION OF DIFLUOROCARBENE WITH BUTADIENE

Shipilov, A. I.,Zabolot-skikh, V. F.,Nefedov, O. M.

, p. 77 - 85 (2007/10/02)

Reaction of butadiene with difluorocarbene, resulting in the formation of difluorobenzenes, and its main steps have been systematically studied.The kinetics of thermal conversions of intermediately formed 2,2-difluorovinylcyclopropane and 2,2,3,3-tetrafluorovinylcyclobutane has been examined.The synthesis of difluorobenzenes has been optimized.The results obtained are used as a basis for domestic technology of production of difluorobenzenes.

Synthesis and aromatization of 2+2 cycloadducts of butadienes and tetrafluoroethylene

Weigert, F. J.,Davis, R. F.

, p. 69 - 84 (2007/10/02)

Passing tetrafluoroethylene (TFE) and hydrocarbon dienes down a hot tube at 600 deg C with a contact time of a few seconds produces substituted fluorobenzenes.Specifically, tetrafluoroethylene and butadiene form 1,2-difluorobenzene.The aromatics produced bythe pyrolysis of TFE and methyl-substituted butadienes do not necessarily result from eliminating HF from 2+4 adducts of the starting materials.Solid-acids such as alumina or silica/alumina accelerate the ring-expansion elimination of the 2+2 cycloadducts.Aromatic products result from the preformed 2+2 cycloadducts at temperatures 200 deg C lower than the corresponding thermal reaction.The solid-acids can also influence product regiochemistry.

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