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56961-36-5

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56961-36-5 Usage

Type of compound

Nitro-substituted derivative of naphthalene

Primary use

Intermediate in the synthesis of various organic compounds and pharmaceuticals

Additional uses

Manufacturing of dyes, pigments, and agricultural chemicals

Physical state

Yellow crystalline solid

Solubility

Insoluble in water, soluble in organic solvents

Safety precautions

Harmful if swallowed, inhaled, or absorbed through the skin

Potential health effects

Can cause irritation to the respiratory system, skin, and eyes

Check Digit Verification of cas no

The CAS Registry Mumber 56961-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,6 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56961-36:
(7*5)+(6*6)+(5*9)+(4*6)+(3*1)+(2*3)+(1*6)=155
155 % 10 = 5
So 56961-36-5 is a valid CAS Registry Number.

56961-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chloro-6-nitronaphthalene

1.2 Other means of identification

Product number -
Other names Naphthalene, 1-chloro-6-nitro-

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:56961-36-5 SDS

56961-36-5Downstream Products

56961-36-5Relevant articles and documents

A remarkably simple and efficient benzannulation reaction

Bull, James A.,Hutchings, Michael G.,Quayle, Peter

, p. 1869 - 1872 (2008/03/12)

(Chemical Equation Presented) On a short fuse: Although fused aromatic rings are common structural motifs in natural products, there are relatively few direct methods for the preparation of such systems from acyclic precursors. An atom-transfer radical cyclization carried out under microwave (MW) irradiation has now been developed which gives rapid access to functionalized aromatic compounds from readily available starting materials (see scheme).

Chlorine-Isotopic Exchange between Lithium Chloride and Nitro-activated 1-Chloronaphthalene in Sulpholane Solution

Attia, Mamdouh,Gore, Peter H.,Morris, Donald F. C.

, p. 1332 - 1343 (2007/10/02)

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