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1-Naphthalenecarbonitrile,3-amino-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91135-40-9

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91135-40-9 Usage

Type of compound

Nitrile derivative of naphthalene

Amino group position

3-position

Common uses

Intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes

Appearance

White to pale yellow solid

Solubility

Soluble in organic solvents

Handling precautions

Can be harmful if ingested, inhaled, or if it comes into contact with the skin.

Check Digit Verification of cas no

The CAS Registry Mumber 91135-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,3 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 91135-40:
(7*9)+(6*1)+(5*1)+(4*3)+(3*5)+(2*4)+(1*0)=109
109 % 10 = 9
So 91135-40-9 is a valid CAS Registry Number.

91135-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-aminonaphthalene-1-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-Cyan-2-naphthylamin

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:91135-40-9 SDS

91135-40-9Downstream Products

91135-40-9Relevant academic research and scientific papers

Dissociation of naphthoic acids in non-aqueous media. Comparison of benzene and naphthalene skeletons

Parik, Patrik,Wolfova, Jitka,Ludwig, Miroslav

, p. 385 - 394 (2007/10/03)

Seven monosubstituted 1-naphthoic acids were synthesized by new or modified procedures, and their dissociation constants were measured potentiometrically at 25 °C in methanol, acetonitrile, dimethylformamide, and pyridine. Dissociation constants of these along with thirteen substituted 1-naphthoic acids and twenty-five substituted 2-naphthoic acids previously studied were measured at 25 °C in ethanol and dimethyl sulfoxide. The pKHA values of 3-and 4-substituted 1-naphthoic acids were treated by simple linear regression and principal component analysis, and the results were used for comparison of model compounds and of corresponding 3-and 4-substituted benzoic acids with the aim of comparison of benzene and naphthalene skeletons. It has been found, the 3 and 4 positions of the 1-naphthyl system can roughly be compared with the meta and para positions of benzene, respectively.

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