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88598-56-5

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88598-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88598-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,9 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88598-56:
(7*8)+(6*8)+(5*5)+(4*9)+(3*8)+(2*5)+(1*6)=205
205 % 10 = 5
So 88598-56-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H15NO2/c22-21(23)18-10-7-12-5-6-14-11-13-3-1-2-4-15(13)16-8-9-17(18)19(12)20(14)16/h5-11H,1-4H2

88598-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-nitro-7,8,9,10-tetrahydrobenzo[a]pyrene

1.2 Other means of identification

Product number -
Other names -

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:88598-56-5 SDS

88598-56-5Downstream Products

88598-56-5Relevant articles and documents

Synthesis, Spectral Analysis, and Mutagenicity of 1-, 3-, and 6-Nitrobenzopyrene

Chou, M. W.,Heflich, R. H.,Casciano, D. A.,Miller, D. W.,Freeman, J. P.,et al.

, p. 1156 - 1161 (2007/10/02)

The mutagenic environmental pollutants 1-, 3-, and 6-nitrobenzopyrene were synthesized.Nitration of 7,8,9,10-tetrahydrobenzopyrene with sodium nitrate in trifluoroacetic acid and acetic anhydride at ambient temperature gave a mixture of 1-, 3-, and 6-nitro-7,8,9,10-tetrahydrobenzopyrene, which was separated by chromatography.Dehydrogenation of the isolated nitrotetrahydrobenzopyrenes with 2,3-dichloro-4,5-dicyano-1,6-benzoquinone produced 1-, 3-, and 6-nitrobenzopyrene in high yield.Comparison of the spectral data of these compounds with those obtained from direct nitration of benzopyrene confirmed that 1- and 3-nitrobenzopyrenes are indeed the minor products of the latter reaction.This confirmation also verifies that 1- and 3-nitrobenzopyrene were the minor nitrated products of benzopyrene formed in model air atmospheres.The 1-, 3-, and 6-nitrobenzopyrene were mutagenic in Salmonella typhimurium tester strains TA98 and TA100 in the presence of a mammalian microsomal (S9) activating system.Both 1- and 3-nitrobenzopyrene, but not 6-nitrobenzopyrene, were also direct-acting mutagens in these strains.However, only 6-nitrobenzopyrene exhibited weak mutagenic activity when tested in Chinese hamster ovary cells, while only 3-nitrobenzopyrene produced a concentration-dependent decrease in cellular survival.

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