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14753-05-0

1-CHLORO-2-METHYLPENTANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14753-05-0 Structure

  • Basic information

    1. Product Name: 1-CHLORO-2-METHYLPENTANE
    2. Synonyms: 2-METHYLPENTYL CHLORIDE
    3. CAS NO:14753-05-0
    4. Molecular Formula: C6H13Cl
    5. Molecular Weight: 120.62
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14753-05-0.mol

  • Chemical Properties

    1. Melting Point: -35.1°C (estimate)
    2. Boiling Point: 120°C(lit.)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 0.8700
    6. Refractive Index: 1.4190-1.4220
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. Water Solubility: Insoluble in water
    10. CAS DataBase Reference: 1-CHLORO-2-METHYLPENTANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-CHLORO-2-METHYLPENTANE(14753-05-0)
    12. EPA Substance Registry System: 1-CHLORO-2-METHYLPENTANE(14753-05-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. RIDADR: 1993
    5. WGK Germany:
    6. RTECS:
    7. HazardClass: 3
    8. PackingGroup: III
    9. Hazardous Substances Data: 14753-05-0(Hazardous Substances Data)

14753-05-0 Usage

Family

Chlorinated hydrocarbons

Physical State

Colorless liquid

Odor

Slightly sweet

Solubility

Insoluble in water

Primary Uses

a. Solvent
b. Intermediate in the synthesis of other compounds
c. Pharmaceutical industry (production of active pharmaceutical ingredients)

Flammability

Flammable

Heating Risk

May emit toxic fumes when heated

Safety Precautions

Proper handling and storage to prevent accidents

Safety Guidelines

Follow safety guidelines and regulations to minimize the risk of exposure

Check Digit Verification of cas no

The CAS Registry Mumber 14753-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,5 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14753-05:
(7*1)+(6*4)+(5*7)+(4*5)+(3*3)+(2*0)+(1*5)=100
100 % 10 = 0
So 14753-05-0 is a valid CAS Registry Number.

14753-05-0SDS

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 6-nitrooctacyclo[10.6.6.63,10.02,11.04,9.013,18.019,24.025,30]triaconta-4,6,8,13,15,17,19,21,23,25,27,29-dodecaene(non-preferred name)

1.2 Other means of identification

Product number -
Other names 1-chloro-2-methyl-pentane

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:14753-05-0 SDS

14753-05-0Downstream Products

14753-05-0Relevant articles and documents

Studies on Sulphochlorination of Paraffins. IX. Regularities of the Sulphochlorination of Branched-chain Paraffins

Estel, D.,Mateew, K.,Pritzkow, W.,Schmidt-Renner, W.

, p. 262 - 268 (2007/10/02)

In the cases of 2-methylbutane and 2-methylpentane the formation of tertiary sulphochlorides in the sulphochlorination of the parent hydrocarbons could be established by means of 13C-n.m.r.-spectroscopy.The relative rates of the various C-H-bonds in 2-methylbutane, 2-methylpentane and 3-methylpentane in the sulphochlorination reaction were determined.The relative rates of the tertiary C-H-bonds in the sulphochlorination were considerably lower than the corresponding values for the chlorination of the branched-chain paraffins.

Alkylation of alkyl, cycloalkyl and aralkyl halides

-

, (2008/06/13)

Alkyl, cycloalkyl or aralkyl halides may be alkylated by treatment with an olefin in the presence of a catalyst comprising a free-radical generating compound such as an organic peroxide and also in the presence of a promoter comprising hydrogen chloride, said alkylation reaction being effected at temperatures at least as high as the decomposition temperature of the free-radical generating compound, to prepare alkylated halide-containing compounds.

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