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146137-78-2

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146137-78-2 Usage

Chemical Properties

clear light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 146137-78-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,3 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 146137-78:
(8*1)+(7*4)+(6*6)+(5*1)+(4*3)+(3*7)+(2*7)+(1*8)=132
132 % 10 = 2
So 146137-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H4F4O/c9-7-2-1-6(8(10,11)12)3-5(7)4-13/h1-4H

146137-78-2 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (A19973)  2-Fluoro-5-(trifluoromethyl)benzaldehyde, 97%   

  • 146137-78-2

  • 1g

  • 274.0CNY

  • Detail
  • Alfa Aesar

  • (A19973)  2-Fluoro-5-(trifluoromethyl)benzaldehyde, 97%   

  • 146137-78-2

  • 5g

  • 818.0CNY

  • Detail
  • Alfa Aesar

  • (A19973)  2-Fluoro-5-(trifluoromethyl)benzaldehyde, 97%   

  • 146137-78-2

  • 25g

  • 3628.0CNY

  • Detail

146137-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-FLUORO-5-(TRIFLUOROMETHYL)BENZALDEHYDE

1.2 Other means of identification

Product number -
Other names 2-Fluoro-5-(trifluoromethyl)benzaldehyde

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:146137-78-2 SDS

146137-78-2Relevant articles and documents

(Oxime)carbamoyl fatty acid amide hydrolase inhibitors

-

, (2008/06/13)

The present invention relates to novel oxime carbamyl derivatives and pharmaceutical compositions comprising said derivatives which inhibit fatty acid amide hydrolase. These pharmaceutical compositions are useful for the treatment of conditions which can be effected by inhibiting fatty acid amide hydrolase including, but not limited to, neuropathic pain, emesis, anxiety, altering feeding behaviors, movement disorders, glaucoma, brain injury, and cardiovascular disease.

3,4-dihydro-4-oxo-3-(2-propenyl)-1-phthalazineacetic acids and derivatives, their preparations and medicines containing them

-

, (2008/06/13)

Novel 3,4-dihydro-4-oxo-3(prop-2-enyl)-1-phtalazineacetic acids and derivatives of formula (I) STR1 in which R1 R2 and R3 are the same or different and stand for H, a halogen or a linear or branched aliphatic, saturated or unsaturated radical, substituted or not by at least one halogen or R4 residue such as defined below, except when R4 is H; R4 and R5 are the same or different and stand for H, a linear or branched aliphatic radical, saturated or unsaturated, an aryl or heteroaryl radical, said radicals being substituted or not by at least one grouping such as fluorine, chlorine, bromine, methyl or trifluoromethyl, where R4 and R5 do not simultaneously denote H; R6 stands for hydroxy or alkoxy radical; R7 stands for H, a halogen, a linear or branched aliphatic saturated or unsaturated radical, an alkoxy radical, said radicals being substituted or not by analiphatic or halogenated radical, a nitro group, a substituted or unsubstituted amino group, S(O)n R8 or a cyano group; n is equal to 0,1 or 2; R8 is an aliphatic, linear or branched radical, an aryl or heteroaryl radical, an amino radical, said radicals being substituted or not by an aliphatic or halogenated radical. This invention also relates to the optional tautomeric forms of said acids and their pharmaceutically acceptable base addition salts. Also described is a process for preparing said compounds and the drugs containing same.

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