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2,4,4,4-tetrachlorobutan-1-ol, with the molecular formula C4H7Cl4O, is a pale yellow liquid chemical compound. It exhibits limited solubility in water but is readily soluble in organic solvents. Recognized for its role as a solvent and a chemical intermediate, it also bears the distinction of being classified as hazardous to the environment and potentially toxic to human health, necessitating careful handling and adherence to safety protocols.

3290-70-8

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3290-70-8 Usage

Uses

Used in Chemical Industry:
2,4,4,4-tetrachlorobutan-1-ol is used as a solvent for various chemical processes, leveraging its solubility in organic solvents to facilitate reactions and dissolution of certain compounds.
2,4,4,4-tetrachlorobutan-1-ol is also used as a chemical intermediate in the synthesis of other substances, contributing to the production of a range of chemical products that may have diverse applications across different industries.
Given its toxic effects and environmental hazards, it is crucial that 2,4,4,4-tetrachlorobutan-1-ol is employed with strict adherence to safety measures, ensuring the protection of both human health and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 3290-70-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3290-70:
(6*3)+(5*2)+(4*9)+(3*0)+(2*7)+(1*0)=78
78 % 10 = 8
So 3290-70-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H6Cl4O/c5-3(2-9)1-4(6,7)8/h3,9H,1-2H2

3290-70-8SDS

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 2,4,4,4-tetrachlorobutan-1-ol

1.2 Other means of identification

Product number -
Other names 2,4,4,4-tetrachloro-butan-1-ol

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:3290-70-8 SDS

3290-70-8Relevant academic research and scientific papers

Addition of trichloromethyl radicals to alkenes: The use of phosphites as hydrogen-atom donors in intermolecular radical reactions

Barks,Gilbert,Parsons,Upeandran

, p. 1719 - 1722 (2007/10/03)

Addition of trichloromethyl radicals (generated from BrCCl3 or CCl4) to a variety of alkenes in the presence of hydrogen-atom donors has been explored. The use of phosphites as hydrogen-atom donors was shown to provide a mild, novel and technically clean approach to trichloroalkanes.

METAL-OXIDE INDUCED REDOX CHAIN ADDITION OF TETRACHLOROMETHANE TO A CARBON-CARBON DOUBLE BOND

Hajek, Milan,Silhavy, Premysl,Malek, Jaroslav

, p. 3488 - 3501 (2007/10/02)

Formation of 1:1 adducts in the addition of tetrachloromethane to a terminal carbon-carbon double bond was investigated at 76-200 deg C.The redox chain addition reaction with 1-octene, electron-deficient alkenes and unconjugated aliphatic dienes induced by catalytic amounts of copper(I) or copper(II) oxides in conjugation with diethylamine or diisopropylamine afforded the corresponding 1:1 adducts up to in 85percent yields.Aliphatic 1,3-dienes underwent redox chain 1,4-addition giving isomeric 1,1,1,5-tetrachloro-3-alkenes.

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