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6996-50-5

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6996-50-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6996-50-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6996-50:
(6*6)+(5*9)+(4*9)+(3*6)+(2*5)+(1*0)=145
145 % 10 = 5
So 6996-50-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H15NO/c1-2-3-4-9-12-13-10-7-5-6-8-11(10)14-12/h5-8H,2-4,9H2,1H3

6996-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-pentyl-1,3-benzoxazole

1.2 Other means of identification

Product number -
Other names BENZOXAZOLE,2-PENTYL

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:6996-50-5 SDS

6996-50-5Downstream Products

6996-50-5Relevant articles and documents

Gold nanoparticles supported on titanium dioxide: An efficient catalyst for highly selective synthesis of benzoxazoles and benzimidazoles

Tang, Lin,Guo, Xuefeng,Yang, Yu,Zha, Zhenggen,Wang, Zhiyong

supporting information, p. 6145 - 6148 (2014/06/09)

A highly efficient and selective reaction for the synthesis of 2-substituted benzoxazoles and benzimidazoles catalyzed by Au/TiO2 has been developed via two hydrogen-transfer processes. This reaction has a good tolerance to air and water, a wide substrate scope, and represents a new avenue for practical C-N and C-O bond formation. More importantly, no additional additives, oxidants and reductants are required for the reaction and the catalyst can be recovered and reused readily. This journal is the Partner Organisations 2014.

Ligand-free copper(II) oxide nanoparticlescatalyzed synthesis of substituted benzoxazoles

Saha, Prasenjit,Ali, Md Ashif,Punniyamurthy, Tharmalingam

, p. 398 - 405 (2014/04/03)

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Ligand-free copper-catalyzed synthesis of substituted benzimidazoles, 2-aminobenzimidazoles, 2-aminobenzothiazoles, and benzoxazoles

Saha, Prasenjit,Ramana, Tamminana,Purkait, Nibadita,Ali, Md. Ashif,Paul, Rajesh,Punniyamurthy, Tharmalingam

supporting information; experimental part, p. 8719 - 8725 (2010/02/28)

(Chemical Equation Presented) The synthesis of substituted benzimidazoles, 2-aminobenzimidazoles, 2-aminobenzothiazoles, and benzoxazoles is described via intramolecular cyclization of o-bromoaryl derivatives using copper(II) oxide nanoparticles in DMSO under air. The procedure is experimentally simple, general, efficient, and free from addition of external chelating ligands. It is a heterogeneous process and the copper(II) oxide nanoparticles can be recovered and recycled without loss of activity. 2009 American Chemical Society.

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