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2,3-dimethyl-2-isopropylbutyryl chloride is a chemical compound characterized by the molecular formula C10H19ClO. It is a colorless liquid with a distinctive pungent odor, known for its reactivity and use as an intermediate in the synthesis of pharmaceuticals and other organic compounds.

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  • 51115-81-2 Structure
  • Basic information

    1. Product Name: 2,3-dimethyl-2-isopropylbutyryl chloride
    2. Synonyms: 2,3-dimethyl-2-isopropylbutyryl chloride
    3. CAS NO:51115-81-2
    4. Molecular Formula: C9H17ClO
    5. Molecular Weight: 176.68368
    6. EINECS: 256-988-0
    7. Product Categories: N/A
    8. Mol File: 51115-81-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 180.4°Cat760mmHg
    3. Flash Point: 47.6°C
    4. Appearance: /
    5. Density: 0.947g/cm3
    6. Vapor Pressure: 0.898mmHg at 25°C
    7. Refractive Index: 1.433
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,3-dimethyl-2-isopropylbutyryl chloride(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,3-dimethyl-2-isopropylbutyryl chloride(51115-81-2)
    12. EPA Substance Registry System: 2,3-dimethyl-2-isopropylbutyryl chloride(51115-81-2)
  • 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: 51115-81-2(Hazardous Substances Data)

51115-81-2 Usage

Uses

Used in Pharmaceutical Manufacturing:
2,3-dimethyl-2-isopropylbutyryl chloride is utilized as a key intermediate in the synthesis of various pharmaceutical drugs. Its role in drug development is crucial due to its ability to react with other compounds to form new medicinal agents.
Used in Organic Synthesis:
In the field of organic chemistry, 2,3-dimethyl-2-isopropylbutyryl chloride serves as a versatile building block for the creation of a wide range of organic compounds. Its reactivity allows chemists to incorporate it into complex molecular structures for various applications.
Used in Chemical Research:
2,3-dimethyl-2-isopropylbutyryl chloride is also employed in chemical research to study reaction mechanisms and to develop new synthetic methodologies. Its unique properties make it a valuable tool for understanding and advancing organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 51115-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,1 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 51115-81:
(7*5)+(6*1)+(5*1)+(4*1)+(3*5)+(2*8)+(1*1)=82
82 % 10 = 2
So 51115-81-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H17ClO/c1-6(2)9(5,7(3)4)8(10)11/h6-7H,1-5H3

51115-81-2SDS

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 2,3-dimethyl-2-propan-2-ylbutanoyl chloride

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-2-isopropylbutyryl chloride

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:51115-81-2 SDS

51115-81-2Downstream Products

51115-81-2Relevant articles and documents

Compositions With A Cooling Effect

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Paragraph 0153, (2019/11/11)

Personal care compositions, such as oral care and skin care compositions comprising one or more coolants. The pleasant cool sensation provided by a coolant is enhanced in terms of quicker onset, greater intensity, impact or longer duration, which improves

Organic Compounds Having Cooling Properties

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Page/Page column 6, (2012/04/23)

Provided are compounds of formula (I) wherein m is 0, 1 or 2; RI is a mono- or bicyclic heterocyclic ring system including one, two or three heteroatoms selected from nitrogen, sulphur and oxygen; R2 is selected from hydrogen, methyl

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