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2-Chloro-3-fluoro-6-methoxybenzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1263378-40-0

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1263378-40-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1263378-40-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,3,3,7 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1263378-40:
(9*1)+(8*2)+(7*6)+(6*3)+(5*3)+(4*7)+(3*8)+(2*4)+(1*0)=160
160 % 10 = 0
So 1263378-40-0 is a valid CAS Registry Number.

1263378-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Chloro-3-fluoro-6-methoxybenzaldehyde

1.2 Other means of identification

Product number -
Other names -

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:1263378-40-0 SDS

1263378-40-0Downstream Products

1263378-40-0Relevant articles and documents

PYRAZOLE DERIVATIVES AS PLASMA KALLIKREIN INHIBITORS

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Page/Page column 59, (2018/01/17)

The present invention provides a selection of compounds of formula (I): (I) compositions comprising such compounds; the use of such compounds in therapy (for example in the treatment or prevention of a disease or condition in which plasma kallikrein activ

CYCLOPROPYLMETHANAMINES AS SELECTIVE 5-HT(2C) RECEPTOR AGONISTS

-

Paragraph 0373-0375, (2016/08/23)

Disclosed are 2-phenyl-cyclopropylmethanamines which are selective 5-HT(2C) receptor agonists and are used in the treatments of diseases and conditions wherein modulation of 5-HT(2C) receptors provides a benefit, such as obesity and psychiatric disorders.

N-((HET)ARYLMETHYL)-HETEROARYL-CARBOXAMIDES COMPOUNDS AS PLASMA KALLIKREIN INHIBITORS,

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Page/Page column 55; 56, (2016/06/14)

The present invention provides compounds of formula (I): (I) compositions comprising such compounds; the use of such compounds in therapy (for example in the treatment or prevention of a disease or condition in which plasma kallikrein activity is implicat

Further Advances in Optimizing (2-Phenylcyclopropyl)methylamines as Novel Serotonin 2C Agonists: Effects on Hyperlocomotion, Prepulse Inhibition, and Cognition Models

Cheng, Jianjun,Giguere, Patrick M.,Schmerberg, Claire M.,Pogorelov, Vladimir M.,Rodriguiz, Ramona M.,Huang, Xi-Ping,Zhu, Hu,McCorvy, John D.,Wetsel, William C.,Roth, Bryan L.,Kozikowski, Alan P.

supporting information, p. 578 - 591 (2016/02/05)

A series of novel compounds with two halogen substituents have been designed and synthesized to further optimize the 2-phenylcyclopropylmethylamine scaffold in the quest for drug-like 5-HT2C agonists. Compound (+)-22a was identified as a potent

FUSED BICYCLIC KINASE INHIBITORS

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Page/Page column 28, (2012/12/13)

Compounds of Formula (I), pharmaceutically acceptable salts thereof, synthesis, intermediates, formulations, and methods of disease treatment therewith, including treatment of cancers, such as tumors driven at least in part by at least one of MET, RON, ALK, IR, or IGF-1R. This Abstract is not limiting of the invention.

Fused Bicyclic Kinase Inhibitors

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Page/Page column 24, (2011/11/30)

Compounds of Formula I, as shown below and defined herein: pharmaceutically acceptable salts thereof, synthesis, intermediates, formulations, and methods of disease treatment therewith, including treatment of cancers, such as tumors driven at least in part by at least one of RON, MET or ALK. This Abstract is not limiting of the invention.

FUSED BICYCLIC KINASE INHIBITORS

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Page/Page column 52-53, (2011/12/02)

Compounds of Formula I, as shown below and defined herein: pharmaceutically acceptable salts thereof, synthesis, intermediates, formulations, and methods of disease treatment therewith, including treatment of cancers, such as but not limited to tumors driven at least in part by at least one of RON, MET, IR, IGF-1 R, or ALK. This Abstract is not limiting of the invention.

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