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9-chloronon-1-ene, also known as 1-chloro-9-nonene, is a chemical compound with the formula C9H17Cl. It is a colorless liquid characterized by a strong, sweet, and slightly pungent odor. 9-chloronon-1-ene is recognized for its reactivity and versatility, making it a significant intermediate in the chemical industry. It is produced through the chlorination of nonene and serves as a precursor to a variety of important chemicals, including detergents, lubricants, and plasticizers.

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  • 872-06-0 Structure
  • Basic information

    1. Product Name: 9-chloronon-1-ene
    2. Synonyms: 1-nonene, 9-chloro-; 9-chloro-1-nonene
    3. CAS NO:872-06-0
    4. Molecular Formula: C9H17Cl
    5. Molecular Weight: 160.69
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 872-06-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 202.5°Cat760mmHg
    3. Flash Point: 73.2°C
    4. Appearance: /
    5. Density: 0.875g/cm3
    6. Vapor Pressure: 0.414mmHg at 25°C
    7. Refractive Index: 1.439
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 9-chloronon-1-ene(CAS DataBase Reference)
    11. NIST Chemistry Reference: 9-chloronon-1-ene(872-06-0)
    12. EPA Substance Registry System: 9-chloronon-1-ene(872-06-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 872-06-0(Hazardous Substances Data)

872-06-0 Usage

Uses

Used in Chemical Synthesis:
9-chloronon-1-ene is used as a key intermediate in the synthesis of various organic compounds due to its reactivity and ability to undergo further chemical reactions.
Used in Detergent Production:
In the detergent industry, 9-chloronon-1-ene is used as a precursor to produce surfactants, which are essential for the cleaning properties of detergents.
Used in Lubricant Formulation:
9-chloronon-1-ene is also utilized in the formulation of lubricants, where it contributes to the viscosity and performance characteristics of the final product.
Used in Plasticizer Manufacturing:
9-chloronon-1-ene is used as a starting material in the production of plasticizers, which are additives that increase the flexibility and workability of plastics.
Safety Considerations:
It is crucial to handle and store 9-chloronon-1-ene with care due to its flammability and potential for causing harm if it comes into contact with the skin or eyes. Proper safety measures should be implemented during its use in industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 872-06-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,7 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 872-06:
(5*8)+(4*7)+(3*2)+(2*0)+(1*6)=80
80 % 10 = 0
So 872-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H17Cl/c1-2-3-4-5-6-7-8-9-10/h2H,1,3-9H2

872-06-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-chloronon-1-ene

1.2 Other means of identification

Product number -
Other names 9-chloro-1-nonene

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:872-06-0 SDS

872-06-0Relevant articles and documents

Method of manufacturing sulfonylhalides unsatd. alkyl

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Paragraph 0041; 0042; 0043, (2017/03/08)

PROBLEM TO BE SOLVED: To provide a production method capable of industrially simply and efficiently providing unsaturated alkyl halides useful as functional compounds, pharmaceuticals, agrochemicals or intermediates thereof.SOLUTION: Vinyl chloride and a Grignard reagent derived from a dihaloalkane represented by the specified general formula (1), where Xand Xeach independently represent Cl, Br or I and n represents an integer from 4 to 12, are reacted in the presence of an iron compound to produce unsaturated alkyl halides represented by the specified general formula (2), where Xrepresents Cl, Br or I and n represents an integer from 4 to 12.

Copper-Catalyzed Cross-Coupling Reaction of Allyl Boron Ester with 1°/2°/3°-Halogenated Alkanes

Wang, Guang-Zu,Jiang, Jian,Bu, Xiao-Song,Dai, Jian-Jun,Xu, Jun,Fu, Yao,Xu, Hua-Jian

supporting information, p. 3682 - 3685 (2015/08/18)

The cross-coupling reaction of allyl boron ester with 1°/2°/3°-halogenated alkanes in the presence of copper has been developed for the first time, which provides a mild and efficient method for the construction of saturated C(sp3)-C(sp3) bonds. This protocol shows excellent compatibility with the nonactivated primary, secondary, and even tertiary halogenated alkanes under mild conditions.

Development of amidine-based sphingosine kinase 1 nanomolar inhibitors and reduction of sphingosine 1-phosphate in human leukemia cells

Kennedy, Andrew J.,Mathews, Thomas P.,Kharel, Yugesh,Field, Saundra D.,Moyer, Morgan L.,East, James E.,Houck, Joseph D.,Lynch, Kevin R.,MacDonald, Timothy L.

supporting information; experimental part, p. 3524 - 3548 (2011/07/07)

Sphingosine 1-phosphate (S1P) is a bioactive lipid that has been identified as an accelerant of cancer progression. The sphingosine kinases (SphKs) are the sole producers of S1P, and thus, SphK inhibitors may prove effective in cancer mitigation and chemosensitization. Of the two SphKs, SphK1 overexpression has been observed in a myriad of cancer cell lines and tissues and has been recognized as the presumptive target over that of the poorly characterized SphK2. Herein, we present the design and synthesis of amidine-based nanomolar SphK1 subtype-selective inhibitors. A homology model of SphK1, trained with this library of amidine inhibitors, was then used to predict the activity of additional, more potent, inhibitors. Lastly, select amidine inhibitors were validated in human leukemia U937 cells, where they significantly reduced endogenous S1P levels at nanomolar concentrations.

Biologically active compounds by catalytic olefin metathesis

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, (2008/06/13)

Biologically active compounds such as pheromones and precursors thereof are produced by catalyzed cross metathesis of dissimilar terminal olefins or of a cyclodiene and a terminal olefin.

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