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2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro- is an organic compound with the chemical formula C12H13N. It is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, with a nitrile group (CN) attached to the 2-position and a tetrahydro (four hydrogen atoms) substitution on the 5,6,7,8-positions. 2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro- is characterized by its unique structure, which combines the properties of naphthalene and nitrile groups, making it a potential intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its specific molecular structure, 2-Naphthaleneacetonitrile, 5,6,7,8-tetrahydro- may exhibit different chemical reactivity and physical properties compared to its parent naphthalene and other related compounds.

3160-18-7

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3160-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3160-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3160-18:
(6*3)+(5*1)+(4*6)+(3*0)+(2*1)+(1*8)=57
57 % 10 = 7
So 3160-18-7 is a valid CAS Registry Number.

3160-18-7SDS

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 [6-(1,2,3,4-tetrahydronaphthalenyl)]acetonitrile

1.2 Other means of identification

Product number -
Other names 5,6,7,8-tetrahydronaphthalene-2-acetonitrile

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:3160-18-7 SDS

3160-18-7Relevant academic research and scientific papers

Antihyperglycemic activity of novel substituted 3H-1,2,3,5-oxathiadiazole 2-oxides

Ellingboe,Alessi,Dolak,Nguyen,Tomer,Guzzo,Bagli,McCaleb

, p. 1176 - 1183 (2007/10/02)

A series of substituted 3H-1,2,3,5-oxathiadiazole-2-oxides (6) was prepared and tested for antihyperglycemic activity in the db/db mouse, a model for type 2 (non-insulin dependent) diabetes mellitus. The oxathiadiazoles 6 were synthesized by a two-step sequence: treatment of a substituted acetonitrile (4) with hydroxylamine to give the corresponding amidoxime (5) and cyclization with thionyl chloride to yield 6. In terms of potency, the 2-naphthalenylmethyl group (as in compound 3) was found to be the optimal substituent in this series. Compound 3 was approximately 5 times more potent than ciglitazone (1).

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