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5-chloro-2,2-dimethyl-pentanenitrile is an organic compound with the chemical formula C7H12ClN. It is a colorless liquid with a molecular weight of 149.63 g/mol. 5-chloro-2,2-dimethyl-pentanenitrile is characterized by the presence of a chloro group (-Cl) at the 5th carbon, two methyl groups (-CH3) at the 2nd carbon, and a nitrile group (-CN) at the end of the pentane chain. It is synthesized through various chemical reactions, such as the addition of hydrogen cyanide to 5-chloro-2,2-dimethyl-2-pentene. 5-chloro-2,2-dimethyl-pentanenitrile is used as an intermediate in the production of pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is essential to handle this compound with care, following proper safety protocols to minimize potential health and environmental risks.

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  • 4207-54-9 Structure
  • Basic information

    1. Product Name: 5-chloro-2,2-dimethyl-pentanenitrile
    2. Synonyms: 5-chloro-2,2-dimethyl-pentanenitrile
    3. CAS NO:4207-54-9
    4. Molecular Formula: C7H12ClN
    5. Molecular Weight: 145.63
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 4207-54-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 227.1°Cat760mmHg
    3. Flash Point: 77.4°C
    4. Appearance: /
    5. Density: 0.978g/cm3
    6. Vapor Pressure: 0.0789mmHg at 25°C
    7. Refractive Index: 1.439
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-chloro-2,2-dimethyl-pentanenitrile(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-chloro-2,2-dimethyl-pentanenitrile(4207-54-9)
    12. EPA Substance Registry System: 5-chloro-2,2-dimethyl-pentanenitrile(4207-54-9)
  • 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: 4207-54-9(Hazardous Substances Data)

4207-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4207-54-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,0 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4207-54:
(6*4)+(5*2)+(4*0)+(3*7)+(2*5)+(1*4)=69
69 % 10 = 9
So 4207-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H12ClN/c1-7(2,6-9)4-3-5-8/h3-5H2,1-2H3

4207-54-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-2,2-dimethylpentanenitrile

1.2 Other means of identification

Product number -
Other names 5-chloro-2,2-dimethyl-valeronitrile

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:4207-54-9 SDS

4207-54-9Relevant articles and documents

Rate constants for the addition of the 2-cyano-2-propyl radical to alkenes in solution

Heberger,Fischer

, p. 249 - 263 (1993)

Absolute rate constants for the addition of the 2-cyano-2-propyl radical to 26 alkenes CH2 = CXY at 315 K were determined in solution by time-resolved electron-spin-resonance spectroscopy. They vary with the alkene substituents from 30 M-1 s-1 to 7′010 M-1 s-1. For styrene the temperature dependence is given by log k/M-1 s-1 = 7.7 - 26.1/Θ where Θ = 2.303 RT in kJ/mol. An analysis of the substituent effects in terms of polar and enthalpic factors reveals a dominant influence of the overall reaction enthalpy.

Cascade cyclization intermolecular dipolar cycloaddition by multi-component couplings-synthesis of indolizidines and pyrrolizidines

Coldham, Iain,Jana, Samaresh,Watson, Luke,Pilgram, Christopher D.

, p. 5408 - 5410 (2008)

A three-component coupling reaction of a primary amine (an amino-acid or amino-ester or hydroxylamine), an alkene or alkyne dipolarophile and an aldehyde bearing a halide as a leaving group has been developed. Condensation of the amine with the aldehyde and cyclization (intramolecular N-alkylation) provides, after decarboxylation or deprotonation, a cyclic azomethine ylide (or nitrone) that undergoes intermolecular dipolar cycloaddition with the dipolarophile. This sets up, in a single step, the bicyclic indolizidine or pyrrolizidine ring system, depending on the length of the tether between the aldehyde and the halide. The reaction is successful with stabilized and non-stabilized azomethine ylides that result from using primary amino-esters or amino-acids, respectively.

SEMICONDUCTING COMPOSITIONS COMPRISING SEMICONDUCTING POLYMERS

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Paragraph 0580-0582, (2019/05/15)

A semiconducting composition comprising a semiconducting polymer and a semiconducting non-polymeric polycyclic compound, wherein the semiconducting polymer comprises units of A and/or B: wherein R1, R2, R5, R6, R7, R8, x, y, p, q, r, R3, R4, R9, R10 and R11 have any of the meanings defined in the description.

ANTI-MUCUS DRUGS AND USES THEREFOR

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Paragraph 0194; 0197, (2015/07/15)

Disclosed are methods of identifying, generating and synthesizing compounds that inhibit MAPK13 activity. In various embodiments, compounds, salts thereof and prodrugs thereof of the present teachings can be useful for the treatment of diseases and disord

THIAZOLYL AND OXAZOLYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS

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Paragraph 00373, (2014/06/11)

Compounds of Formula (I) or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.

N-(MONOCYCLIC ARYL),N'-PYRAZOLYL-UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS

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Paragraph 00557, (2014/06/11)

Compounds of Formula (I) or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.

BICYCLIC HETEROARYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS

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Paragraph 00488, (2014/06/11)

Compounds of Formula I or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis and pelvic pain syndrome.

N-BICYCLIC ARYL,N'-PYRAZOLYL UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS

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Paragraph 00485, (2014/06/11)

Compounds of Formula (I): or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.

N-(ARYLALKYL)-N'-PYRAZOLYL-UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS

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Paragraph 00686, (2014/06/11)

Compounds of Formula I or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C, X, Ra, Rb, Rc, Rd and n are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.

BICYCLIC UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS USEFUL FOR THE TREATMENT OF PAIN

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Paragraph 00626, (2014/06/11)

Compounds of Formula I: or stereoisomers, tautomers, or pharmaceutically acceptable salts, solvates or prodrugs thereof, wherein Ring A, Ring C and X are as defined herein, are inhibitors of TrkA kinase and are useful in the treatment of diseases which can be treated with a TrkA kinase inhibitor such as pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis and pelvic pain syndrome.

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