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78832-54-9

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78832-54-9 Usage

Uses

2-Naphthol-d7 has been used as a reactant for the preparation of stable isotope-labeled internal standards of PAH metabolites from urine of smokers and nonsmokers.

Check Digit Verification of cas no

The CAS Registry Mumber 78832-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,3 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 78832-54:
(7*7)+(6*8)+(5*8)+(4*3)+(3*2)+(2*5)+(1*4)=169
169 % 10 = 9
So 78832-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H/i1D,2D,3D,4D,5D,6D,7D

78832-54-9SDS

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 1,3,4,5,6,7,8-heptadeuterionaphthalen-2-ol

1.2 Other means of identification

Product number -
Other names 2-Naphthol-1,3,4,5,6,7,8-d7

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:78832-54-9 SDS

78832-54-9Upstream product

78832-54-9Relevant articles and documents

Uranyl-Sensitized Photochemical Oxidation of Naphthalene by Molecular Oxygen. Role of Electron Transfer

Mao, Yun,Bakac, Andreja

, p. 7929 - 7933 (1997)

Naphthalene quenches the excited state *UO2(2+) in two parallel pathways: oxidation to naphthalene radical cation, C10H8(.+) (Φ = 0.3), and exciplex formation.The overall rate constant in aqueous acetonitrile containing 0.1 M H3PO4 has a value kq = 2.20E9 M-1 s-1.In the presence of O2, a portion of c10H8(.+) is converted to 2-formylcinnamaldehyde and several other products, the rest reacting with UO2(1+) by back electron transfer.

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