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3007-96-3

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3007-96-3 Usage

Derived from

Naphthalene (a common aromatic hydrocarbon)

Uses

Production of fragrances, flavors, and other industrial applications; fragrance ingredient in cosmetic products; solvent in manufacturing of cellulose esters, lacquers, and plasticizers

Physical properties

Clear, colorless to pale yellow liquid; low vapor pressure; relatively stable under normal conditions

Odor

Slightly sweet, floral odor

Check Digit Verification of cas no

The CAS Registry Mumber 3007-96-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3007-96:
(6*3)+(5*0)+(4*0)+(3*7)+(2*9)+(1*6)=63
63 % 10 = 3
So 3007-96-3 is a valid CAS Registry Number.

3007-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name propyl naphthalene-1-carboxylate

1.2 Other means of identification

Product number -
Other names n-Propyl-1-naphthoat

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:3007-96-3 SDS

3007-96-3Downstream Products

3007-96-3Relevant articles and documents

Highly regioselective synthesis of 1,3-diiodonaphthalene derivatives via a sequential cascade iodocyclization

Wang, Li-Jing,Zhu, Hai-Tao,Lu, Lei,Yang, Fang,Liu, Xue-Yuan,Liang, Yong-Min

, p. 1990 - 1993 (2012/06/01)

A novel and flexible sequentially cascade iodocyclization for the synthesis of highly substituted 1,3-diiodinated naphthalene derivatives in up to 99% yield under mild conditions is reported. The dihalogenated moiety can be readily introduced into the naphthalenes in a position that is usually not easily functionalized.

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