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naphthalene-1,8-diyldimethanethiol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60948-99-4

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60948-99-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60948-99-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,4 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 60948-99:
(7*6)+(6*0)+(5*9)+(4*4)+(3*8)+(2*9)+(1*9)=154
154 % 10 = 4
So 60948-99-4 is a valid CAS Registry Number.

60948-99-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [8-(sulfanylmethyl)naphthalen-1-yl]methanethiol

1.2 Other means of identification

Product number -
Other names 1,8-naphthalenedimethanethiol

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:60948-99-4 SDS

60948-99-4Relevant academic research and scientific papers

Synthesis of Potentially Basic Hydrocarbons by Sulphur Extrusion and/or Bis-Wittig Reactions. Two Syntheses of Benzindenophenalene and a New Synthesis of Dibenzonaphthacene (Zethrene)

Kemp, William,Storie, Iain T.,Tulloch, Charles D.

, p. 2812 - 2817 (2007/10/02)

Macrocyclic bis-sulphides have been prepared from 1,2-, 2,3-, and 1,8-bis(bromomethyl)naphthalenes.Methylation of the bis-sulphides, followed by the Stevens rearrangement, gave the corresponding carbocycles with extra-annular sulphide groups; removal of these sulphide groups by Hofmann elimination led to spontaneous trans-annular condensation.Using this general method, two hydrocarbons were synthesized: benzindenophenalene and dibenzonaphthacene (or zethrene).An alternative synthetic route led to the synthesis of benzindenophenalene, using the Wittig reaction between naphthalene-2,3-carbaldehyde and 1,8-bis(triphenylphosphoniomethyl)naphthalene dibromide.

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