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2-(5-Bromo-2-fluorophenyl)acetaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

844904-33-2

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844904-33-2 Usage

Molecular weight

213.04 g/mol

Type of compound

Aldehyde derivative

Usage

Pharmaceutical, agrochemical, and materials science industries

Potential

Medicinal properties and drug development and synthesis

Reactivity

Versatile properties and reactivity for the production of other chemicals and materials

Value

Valuable intermediate for the synthesis of various complex organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 844904-33-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,4,9,0 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 844904-33:
(8*8)+(7*4)+(6*4)+(5*9)+(4*0)+(3*4)+(2*3)+(1*3)=182
182 % 10 = 2
So 844904-33-2 is a valid CAS Registry Number.

844904-33-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(5-bromo-2-fluorophenyl)acetaldehyde

1.2 Other means of identification

Product number -
Other names (5-bromo-2-fluorophenyl)acetaldehyde

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:844904-33-2 SDS

844904-33-2Relevant academic research and scientific papers

IKK-β SERINE-THREONINE PROTEIN KINASE INHIBITORS

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Page/Page column 47-48, (2008/12/05)

Compounds of formula (IA) or (IB) are inhibitors of IkB kinase (IKK) activity, and are useful in the treatment of autoimmune and inflammatory diseases: Formula (A) and (B) wherein R7 is hydrogen or optionally substituted (C1-C6)alkyl; ring A is an optionally substituted aryl or heteroaryl ring of 5-13 ring atoms; Z is (a) a radical of formula R1R2CHNH-Y-L1-X1-(CH2)Z- wherein: z is 0 or 1; R1 is a carboxylic acid group (-COOH), or an ester group which is hydrolysable by one or more intracellular esterase enzymes to a carboxylic acid group; R2 is the side chain of a natural or non- natural alpha amino acid; Y is a bond, -C(=O)-, -S(=O)2-, -C(=O)O-, -C(=O)NR3-, - C(=S)-NR3, -C(=NH)-NR3 or -S(=O)2NR3- wherein R3 is hydrogen or optionally substituted C1-C6 alkyl; L1 is a divalent linker radical of formula -(Alk1)m(Q)n(Alk2)p- wherein m, n, p, Q, AIk1 and AIk2 are as defined in the claims.

QUINOLINE AND QUINAZOLINE DERIVATIVES HAVING AFFINITY FOR 5HT1-TYPE RECEPTORS

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Page/Page column 92, (2008/06/13)

Compounds of formula (I) and pharmaceutically acceptable salts thereof are provided: wherein R1, m, X, R2, n, W, p, Y, Z, R3, R4, R5 and q have the meanings as defined in the description. Methods of preparation and uses thereof in therapy, particularly for CNS disorders such as depression or anxiety, are also disclosed.

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