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21900-39-0

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21900-39-0 Usage

Chemical Properties

light yellow liquid

Check Digit Verification of cas no

The CAS Registry Mumber 21900-39-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,0 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 21900-39:
(7*2)+(6*1)+(5*9)+(4*0)+(3*0)+(2*3)+(1*9)=80
80 % 10 = 0
So 21900-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClFO/c1-5-2-3-6(10)4-7(5)8(9)11/h2-4H,1H3

21900-39-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (L13750)  5-Fluoro-2-methylbenzoyl chloride, 98%   

  • 21900-39-0

  • 1g

  • 332.0CNY

  • Detail
  • Alfa Aesar

  • (L13750)  5-Fluoro-2-methylbenzoyl chloride, 98%   

  • 21900-39-0

  • 5g

  • 1178.0CNY

  • Detail
  • Aldrich

  • (654779)  5-Fluoro-2-methylbenzoylchloride  97%

  • 21900-39-0

  • 654779-1G

  • 532.35CNY

  • Detail
  • Aldrich

  • (654779)  5-Fluoro-2-methylbenzoylchloride  97%

  • 21900-39-0

  • 654779-5G

  • 1,943.37CNY

  • Detail

21900-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Fluoro-2-methylbenzoyl chloride

1.2 Other means of identification

Product number -
Other names 5-Fluoro-2-methyl benzoylchloride

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:21900-39-0 SDS

21900-39-0Relevant articles and documents

Cobalt-Catalyzed C-H Iodination of Aromatic Amides with Molecular Iodine through the Use of a 2-Aminophenyloxazoline-Based Bidentate-Chelation System

Kommagalla, Yadagiri,Chatani, Naoto

, p. 5971 - 5976 (2019)

The cobalt-catalyzed chelation-assisted C-H iodination of aromatic amides using molecular iodine as an iodinating reagent is reported. The reaction is carried out in an atmosphere of air and uses Co(OAc)2·4H2O as an efficient catalys

N-Heterocyclic Carbene Catalyzed Photoenolization/Diels–Alder Reaction of Acid Fluorides

Agrawal, Arush,G?tze, Jan P.,Golz, Paul,Hopkinson, Matthew N.,Mavroskoufis, Andreas,Rajes, Keerthana,Ru?, Vincent

supporting information, p. 3190 - 3194 (2020/01/24)

The combination of light activation and N-heterocyclic carbene (NHC) organocatalysis has enabled the use of acid fluorides as substrates in a UVA-light-mediated photochemical transformation previously observed only with aromatic aldehydes and ketones. Stoichiometric studies and TD-DFT calculations support a mechanism involving the photoactivation of an ortho-toluoyl azolium intermediate, which exhibits “ketone-like” photochemical reactivity under UVA irradiation. Using this photo-NHC catalysis approach, a novel photoenolization/Diels–Alder (PEDA) process was developed that leads to diverse isochroman-1-one derivatives.

IMIDAZOTRIAZINONE COMPOUNDS

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Paragraph 0583; 0584; 0585, (2013/10/08)

The present invention provides imidazotriazinone compounds which are inhibitors of phosphodiesterase 9 and pharmaceutically acceptable salt thereof. The present invention further provides processes, pharmaceutical compositions, pharmaceutical preparations and pharmaceutical use of the compounds in the treatment of PDE9 associated diseases or disorders in mammals, including humans.

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