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41332-02-9

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41332-02-9 Usage

Description

1-(2-CHLOROETHYL)NAPHTHALENE, also known as 1-(1-Naphthyl)-2-chloroethane with the CAS number 41332-02-9, is a chemical compound that is useful in organic synthesis. It is a colorless liquid and plays a significant role in the creation of various organic compounds.

Uses

1. Used in Organic Synthesis:
1-(2-CHLOROETHYL)NAPHTHALENE is used as a key intermediate for the synthesis of various organic compounds. Its unique structure allows it to be a versatile building block in the development of new molecules with potential applications in different industries.
2. Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1-(2-CHLOROETHYL)NAPHTHALENE is used as a starting material for the development of new drugs. Its chemical properties make it suitable for the creation of molecules with potential therapeutic effects.
3. Used in Chemical Research:
1-(2-CHLOROETHYL)NAPHTHALENE is also utilized in chemical research to study the properties and reactions of naphthalene-based compounds. This helps researchers understand the behavior of these compounds and develop new methods for their synthesis and application.
4. Used in Material Science:
In the field of material science, 1-(2-CHLOROETHYL)NAPHTHALENE can be used to develop new materials with specific properties. Its incorporation into polymers or other materials can lead to the creation of materials with enhanced characteristics, such as improved stability or reactivity.
5. Used in Dye and Pigment Industry:
1-(2-CHLOROETHYL)NAPHTHALENE can be used as a precursor for the synthesis of dyes and pigments. Its unique structure can contribute to the development of new colors and shades, expanding the range of available dyes and pigments for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 41332-02-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,3 and 2 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41332-02:
(7*4)+(6*1)+(5*3)+(4*3)+(3*2)+(2*0)+(1*2)=69
69 % 10 = 9
So 41332-02-9 is a valid CAS Registry Number.

41332-02-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-Chloroethyl)naphthalene

1.2 Other means of identification

Product number -
Other names 1-(2-CHLOROETHYL)NAPHTHALENE

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:41332-02-9 SDS

41332-02-9Relevant articles and documents

Chemoselective Homologation-Deoxygenation Strategy Enabling the Direct Conversion of Carbonyls into (n+1)-Halomethyl-Alkanes

Citarella, Andrea,Holzer, Wolfgang,Ielo, Laura,Langer, Thierry,Miele, Margherita,Pace, Vittorio,Urban, Ernst,Zehl, Martin

supporting information, p. 7629 - 7634 (2020/10/12)

The sequential installation of a carbenoid and a hydride into a carbonyl, furnishing halomethyl alkyl derivatives, is reported. Despite the employment of carbenoids as nucleophiles in reactions with carbon-centered electrophiles, sp3-type alkyl halides remain elusive materials for selective one-carbon homologations. Our tactic levers on using carbonyls as starting materials and enables uniformly high yields and chemocontrol. The tactic is flexible and is not limited to carbenoids. Also, diverse carbanion-like species can act as nucleophiles, thus making it of general applicability.

Gallium-catalyzed reductive chlorination of carboxylic acids with copper(II) chloride

Sakai, Norio,Nakajima, Takumi,Yoneda, Shinichiro,Konakahara, Takeo,Ogiwara, Yohei

, p. 10619 - 10623 (2015/02/19)

Described herein is the direct chlorination of carboxylic acids using copper(II) chloride via a gallium(III)-catalyzed reduction in the presence of a hydrosiloxane. During this reductive chlorination, the counteranions of CuCl2 functioned as a chloride source.

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