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13947-96-1

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13947-96-1 Usage

General Description

1-(trichloromethyl)-4-(trifluoromethyl)benzene, also known as TCTB, is a chemical compound with the molecular formula C9H4Cl3F3. It is a colorless, odorless solid that is insoluble in water but soluble in organic solvents. TCTB is primarily used as an intermediate in the synthesis of other chemicals, and it is also used as an indicator for the detection of explosives. It is a highly reactive compound, and caution should be taken when handling it, as it can react violently with other chemicals. TCTB is considered to be harmful if ingested, inhaled, or in contact with skin, and it has potential long-term effects on aquatic life. Overall, TCTB is a versatile chemical with various industrial applications, but it should be handled and used with care to avoid any potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 13947-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,4 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13947-96:
(7*1)+(6*3)+(5*9)+(4*4)+(3*7)+(2*9)+(1*6)=131
131 % 10 = 1
So 13947-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H4Cl3F3/c9-7(10,11)5-1-3-6(4-2-5)8(12,13)14/h1-4H

13947-96-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Trichloromethyl)-4-(trifluoromethyl)benzene

1.2 Other means of identification

Product number -
Other names 4-Trichlormethyl-benzotrifluorid

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:13947-96-1 SDS

13947-96-1Relevant articles and documents

Catalytic halodefluorination of aliphatic carbon-fluorine bonds

Goh, Kelvin K.K.,Sinha, Arup,Fraser, Craig,Young, Rowan D.

, p. 42708 - 42712 (2016/05/19)

A variety of halosilanes, in conjunction with aluminum catalysts, convert fluorocarbons into higher halocarbons. Bromination and iodination of fluorocarbons are more effective than chlorination in terms of yield and activity. The mechanism for the reaction is investigated utilizing experimental and computational evidence and preliminary results suggest an alternate mechanism to that reported for the related hydrodefluorination reaction.

Method for preparing trichloromethyl-trifluoromethyl-benzenes

-

, (2008/06/13)

A process for the preparation of a trichloromethyl-trifluoromethyl-benzene of the formula STR1 wherein R1 and R2 are identical or different and represent hydrogen, fluorine or chlorine, By contacting at least one molecule of the formula STR2 wherein R1 and R2 are as previously identified, m and n are independently 0 to 3 With another molecule of the formula STR3 wherein M AND N ARE INDEPENDENTLY 0 TO 3 In the presence of a halogen transfer catalyst, optionally in the presence of a promoter.

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