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Benzoxazole, 5-nitro-2-[(4-nitrophenyl)methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104233-74-1

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104233-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104233-74-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,2,3 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 104233-74:
(8*1)+(7*0)+(6*4)+(5*2)+(4*3)+(3*3)+(2*7)+(1*4)=81
81 % 10 = 1
So 104233-74-1 is a valid CAS Registry Number.

104233-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-nitro-2-(4-nitrobenzyl)benzoxazole

1.2 Other means of identification

Product number -
Other names 5-Nitro-2-(4-nitro-benzyl)-benzooxazole

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:104233-74-1 SDS

104233-74-1Downstream Products

104233-74-1Relevant academic research and scientific papers

Vibrational spectroscopic (FT-IR, FT-Raman, 1H NMR and UV) investigations and computational study of 5-nitro-2-(4-nitrobenzyl) benzoxazole

Bhagyasree,Varghese, Hema Tresa,Panicker, C. Yohannan,Samuel, Jadu,Van Alsenoy, Christian,Bolelli, Kayhan,Yildiz, Ilkay,Aki, Esin

, p. 99 - 113 (2013)

The optimized molecular structure, vibrational frequencies, corresponding vibrational assignments of 5-nitro-2-(4-nitrobenzyl) benzoxazole have been investigated experimentally and theoretically using Gaussian09 software package. Potential energy distribu

Synthesis and HIV-1 reverse transcriptase inhibitor activity of some 2,5,6-substituted benzoxazole, benzimidazole, benzothiazole and oxazolo (4,5-b)pyridine derivatives

Akbay, Ayseguel,Oeren, Ilkay,Temiz-Arpaci, Oezlem,Aki-Sener, Esin,Yalcin, Ismail

, p. 266 - 271 (2007/10/03)

In this study, the synthesis of some benzoxazoles and their analogues were described and their antiviral activities were studied together with the previously synthesized 2,5,6-trisubstituted benzoxazole, benzothiazole, benzimidazole and oxazolo(4,5-b)pyridine derivatives. The reverse transcriptase (RT) inhibitory activity of these compounds was determined using a commercial kit and assay system which utilizes the scintillation proximity assay principle. The results are concentration at which the compound inhibits RT activity by 50%). The compounds inhibited the in vitro binding of thymidine to the RT enzyme exhibiting IC50 values between 6.3 × 105 μmol/l-0.34 μmol/l and their activities were compared to some standard drugs such as 3′-azido-2′,3′-dideoxythymidine triphosphate and dideoxythymidine triphosphate.

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