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149947-15-9

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149947-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 149947-15-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,9,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149947-15:
(8*1)+(7*4)+(6*9)+(5*9)+(4*4)+(3*7)+(2*1)+(1*5)=179
179 % 10 = 9
So 149947-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BrFO/c8-7-5(4-10)2-1-3-6(7)9/h1-4H

149947-15-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H64650)  3-Bromo-2-fluorobenzaldehyde, 97%   

  • 149947-15-9

  • 5g

  • 412.0CNY

  • Detail
  • Alfa Aesar

  • (H64650)  3-Bromo-2-fluorobenzaldehyde, 97%   

  • 149947-15-9

  • 25g

  • 1646.0CNY

  • Detail
  • Alfa Aesar

  • (H64650)  3-Bromo-2-fluorobenzaldehyde, 97%   

  • 149947-15-9

  • 100g

  • 6586.0CNY

  • Detail

149947-15-9SDS

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-Bromo-3-Fluorobenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-bromo-2-fluorobenzaldehyde

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:149947-15-9 SDS

149947-15-9Relevant articles and documents

Enantioselective Total Synthesis of Beraprost Using Organocatalyst

Umemiya, Shigenobu,Sakamoto, Daisuke,Kawauchi, Genki,Hayashi, Yujiro

, p. 1112 - 1115 (2017)

A convergent and enantioselective total synthesis of the most active isomer of beraprost was achieved in 17 pots. A unique tricyclic core in beraprost was synthesized efficiently by utilizing the asymmetric organocatalyst-mediated formal [3 + 2] cycloaddi

N-(piperidin-4-yl)benzo[b]thiophenecarboxamide derivatives, preparation method therof, and pharmaceutical composition for use in preventing or treating Urotensin-Ⅱ receptor activity related diseases containing the same as an active ingredient

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Paragraph 0181; 0182; 0183; 0184, (2016/10/10)

The present invention relates to N-(piperidin-4-yl)benzo[b]thiophenecarboxamide derivatives, a manufacturing method thereof, and a pharmaceutical composition for preventing or treating urotensin-II receptor activity-related diseases comprising the same as an active ingredient. The N-(piperidin-4-yl)benzo[b]thiophenecarboxamide derivatives can be usefully used for preventing or treating urotensin-II receptor activity-related diseases such as congestive heart failure, ischemic heart, myocardial infarction, cardiomegaly, fibrosis cordis, coronary artery disease, arteriosclerosis, hypertension, asthma, renal failure, diabetes, vasculitis, neurodegenerative disease, stroke, pain, depressive disorder, psychosis, cancer, etc., by acting as an antagonist with respect to a urotensin-II receptor.COPYRIGHT KIPO 2016

SULPHONYLAMINOPYRROLIDINONE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION

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Page/Page column 42; 43, (2013/07/05)

The invention relates to new sulphonylaminopyrrolidinone compounds having antithrombotic activity which, in particular, inhibit blood clotting factor IXa and/ or factor Xa, to processes for their preparation and to use thereof as drugs.

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