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1185742-22-6

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1185742-22-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1185742-22-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,7,4 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1185742-22:
(9*1)+(8*1)+(7*8)+(6*5)+(5*7)+(4*4)+(3*2)+(2*2)+(1*2)=166
166 % 10 = 6
So 1185742-22-6 is a valid CAS Registry Number.

1185742-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5(3)-(4-fluorophenyl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 5-(4-Fluorophenyl)-1H-pyrazole

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:1185742-22-6 SDS

1185742-22-6Downstream Products

1185742-22-6Relevant articles and documents

Molybdenum-silver co-catalyzed cycloaddition of alkynes with: N -isocyanoiminotriphenylphosphorane (NIITP): An efficient strategy for the synthesis of monosubstituted pyrazoles

Mi, Pengbing,Lang, Jiajia,Lin, Shaojian

, p. 7986 - 7989 (2019)

A new molybdenum-silver co-catalyzed [3+2] cycloaddition of alkynes with N-isocyanoiminotriphenylphosphorane (NIITP) has been described. The NIITP serves as a non-toxic, facile "CNN" source. Over 30 substrates were successfully converted to the desired compounds in good to excellent yields.

Discovery and in vitro and in vivo profiles of N-ethyl-N-[2-[3-(5-fluoro-2-pyridinyl)-1H-pyrazol-1-yl]ethyl]-2-(2H-1,2,3-triazol-2-yl)-benzamide as a novel class of dual orexin receptor antagonist

Suzuki, Ryo,Nozawa, Dai,Futamura, Aya,Nishikawa-Shimono, Rie,Abe, Masahito,Hattori, Nobutaka,Ohta, Hiroshi,Araki, Yuko,Kambe, Daiji,Ohmichi, Mari,Tokura, Seiken,Aoki, Takeshi,Ohtake, Norikazu,Kawamoto, Hiroshi

, p. 1260 - 1275 (2015/03/04)

Orexins play an important role in sleep/wake regulation, and orexin receptor antagonists are a focus of novel therapy for the treatment of insomnia. We identified 27e (TASP0428980) as a potent dual orexin receptor antagonist through the systematic modification of our original designed lead A. We demonstrated the potent sleep-promoting effects of 27e at ip dose of 3 mg/kg in a rat polysomnogram study. 27e exhibited relatively short half-life profiles in rats and dogs. Furthermore, accumulating evidence regarding ADME profiles indicates that the predicted human half-life of 27e should be 1.2-1.4 h. These data indicated that 27e has a short-acting hypnotic property, suggesting that 27e might be useful for treating primary insomnia while exhibiting a low risk of next-day residual somnolence. Thus, 27e and its related compounds should be further evaluated to enable advancement to clinical trials.

An efficient solvent-free synthesis of NH-pyrazoles from β-dimethylaminovinylketones and hydrazine on grinding

Longhi, Kelvis,Moreira, Dayse N.,Marzari, Mara R.B.,Floss, Vagner M.,Bonacorso, Helio G.,Zanatta, Nilo,Martins, Marcos A.P.

supporting information; experimental part, p. 3193 - 3196 (2010/08/05)

A series of NH-pyrazoles was efficiently synthesized from the reaction of β-dimethylaminovinylketones ([R1C(O)C(R2){double bond, long}CHN(Me2)], where R1 = Me, Ph, 3-MeO-Ph, 4-Me-Ph, 4-MeO-Ph, 4-F-Ph, 4-Cl-Ph, 4

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