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885270-14-4

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885270-14-4 Usage

General Description

7-Bromobenzo[d]oxazole is a chemical compound with the molecular formula C7H4BrNO. It is a heterocyclic aromatic organic compound containing a benzene ring fused to an oxazole ring with a bromine substituent at the 7-position. 7-Bromobenzo[d]oxazole is commonly used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also employed in research laboratories as a versatile starting material for the development of new chemical entities. 7-Bromobenzo[d]oxazole is known for its high reactivity and versatility, making it a valuable asset in organic synthesis and drug discovery efforts.

Check Digit Verification of cas no

The CAS Registry Mumber 885270-14-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,2,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 885270-14:
(8*8)+(7*8)+(6*5)+(5*2)+(4*7)+(3*0)+(2*1)+(1*4)=194
194 % 10 = 4
So 885270-14-4 is a valid CAS Registry Number.

885270-14-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Bromobenzo[d]oxazole

1.2 Other means of identification

Product number -
Other names 7-bromo-1,3-benzoxazole

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:885270-14-4 SDS

885270-14-4Downstream Products

885270-14-4Relevant articles and documents

Synthesis of Highly Functionalized N,N-Diarylamides by an Anodic C,N-Coupling Reaction

D?rr, Maurice,Lips, Sebastian,Martínez-Huitle, Carlos Alberto,Schollmeyer, Dieter,Franke, Robert,Waldvogel, Siegfried R.

supporting information, p. 7835 - 7838 (2019/05/21)

We report an innovative, sustainable and straightforward protocol for the synthesis of N,N-diarylamides equipped with nonprotected hydroxyl groups by using electrosynthesis. The concept allows the application of various substrates furnishing diarylamides with yields up to 57 % within a single and direct electrolytic protocol. The method is thereby easy to conduct in an undivided cell with constant current conditions offering a versatile and short-cut alternative to conventional pathways.

IMIDAZO [1,5-A]PYRIMIDINYL CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS

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Paragraph 00579, (2017/11/04)

The invention provides substituted imidazo[1,5-a]pyrimidinyl carboxamide and related organic compounds, compositions containing such compounds, medical kits, and methods for using such compounds and compositions to treat medical disorders, e.g., Gaucher disease, Parkinson's disease, Lewy body disease, dementia, or multiple system atrophy, in a patient. Exemplary substituted imidazo[1,5-a]pyrimidinyl carboxamide compounds described herein include substituted 2-heterocyclyl-4-alkyl-imidazo[1,5-a]pyrirnidine-8-carboxamide compounds and variants thereof.

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