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10503-96-5

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10503-96-5 Usage

General Description

2-Chloroethyl n-butyl ether is a colorless and aromatic liquid formed through the reaction of 2-chloroethanol and n-butyl. Its molecular formula is C6H13ClO, indicating the presence of carbon, hydrogen, chlorine, and oxygen atoms in its structure. This chemical compound is primarily used in the synthesis of other chemicals, reacting as an intermediate in organic chemistry. The substance has a moderately low boiling point and a relatively high molecular weight. It should be handled carefully due to potential health hazards; it may cause skin or eye irritation, and prolonged exposure may lead to respiratory issues.

Check Digit Verification of cas no

The CAS Registry Mumber 10503-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10503-96:
(7*1)+(6*0)+(5*5)+(4*0)+(3*3)+(2*9)+(1*6)=65
65 % 10 = 5
So 10503-96-5 is a valid CAS Registry Number.

10503-96-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Butyl 2-Chloroethyl Ether

1.2 Other means of identification

Product number -
Other names 2-Chloroethyl Butyl Ether

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:10503-96-5 SDS

10503-96-5Relevant articles and documents

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Lee,Nolan

, p. 1331,1333 (1966)

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Branch hydroxyoxaalkylmelamine chain and its use has compd.

-

Paragraph 0117, (2018/07/28)

PROBLEM TO BE SOLVED: To provide a means capable of lowering the melting point or the glass transition point of a compound having straight chain alkyl chain or a compound having straight chain oxaalkyl chain and also lowering the viscosity including the kinematic viscosity or the like, and to provide a compound obtained by the means and a use of the compound. SOLUTION: The compound has an oxaalkyl chain which has at least one side chain, in a molecule. COPYRIGHT: (C)2012,JPOandINPIT

Preparation of Alkyl Chlorides, Acid Chlorides, and Amides Using Polymer-Supported Phosphines and Carbon Tetrachloride: Mechanism of These Reactions

Harrison, Charles R.,Hodge, Philip,Hunt, Barry J.,Khoshdel, Ezzatollah,Richardson, Graham

, p. 3721 - 3728 (2007/10/02)

Alcohols and thiols were converted into alkyl chlorides, carboxylic acids were converted into acid chlorides, and mixtures of carboxylic acids and amines were converted into amides by reaction with carbon tetrachloride and 1percent cross-linked polystyrenes containing phosphine residues.Some of these conversions were also effected by using a linear polymer containing phosphine residues.The reactions proceed in high yield, and isolation of the products is facilitated by the ready removal of all the polymer-supported species.The mechanism of the reactions between triphenylphosphine, carbon tetrachloride, and alcohols is complex, but the polymer-supported reactions appear to follow analogous pathways to the low molecular weight reactions as judged by the yields of chloroform and the number of equivalents of phosphine consumed per mole of alkyl chloride produced.The mechanism requires polymer-supported groups reacting together.The slow step in the reactions appears to be the generation of the chlorinating species.The polymer-supported reactions are faster than those using triphenylphosphine or 4-(diphenylphosphinyl)isopropylbenzene.It is suggested that this is due to a microenvironmental effect.

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