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1,3-Cyclopentanediol,1,4-dimethyl-3-(1-methylethyl)-,(1alpha,3alpha,4bta)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1,3-Cyclopentanediol,1,4-dimethyl-3-(1-methylethyl)-,(1alpha,3alpha,4bta)-(9CI)

    Cas No: 189170-44-3

  • USD $ 1.9-2.9 / Gram

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  • 189170-44-3 Structure
  • Basic information

    1. Product Name: 1,3-Cyclopentanediol,1,4-dimethyl-3-(1-methylethyl)-,(1alpha,3alpha,4bta)-(9CI)
    2. Synonyms: 1,3-Cyclopentanediol,1,4-dimethyl-3-(1-methylethyl)-,(1alpha,3alpha,4bta)-(9CI)
    3. CAS NO:189170-44-3
    4. Molecular Formula: C10H20O2
    5. Molecular Weight: 172.2646
    6. EINECS: N/A
    7. Product Categories: ISOPROPYL
    8. Mol File: 189170-44-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,3-Cyclopentanediol,1,4-dimethyl-3-(1-methylethyl)-,(1alpha,3alpha,4bta)-(9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Cyclopentanediol,1,4-dimethyl-3-(1-methylethyl)-,(1alpha,3alpha,4bta)-(9CI)(189170-44-3)
    11. EPA Substance Registry System: 1,3-Cyclopentanediol,1,4-dimethyl-3-(1-methylethyl)-,(1alpha,3alpha,4bta)-(9CI)(189170-44-3)
  • 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: 189170-44-3(Hazardous Substances Data)

189170-44-3 Usage

Explanation

A cyclic diol is a type of organic compound that contains a ring structure with two hydroxyl (OH) groups attached to it.
3. Cyclopentane Ring

Explanation

The compound has a five-membered carbon ring, known as a cyclopentane ring, as its core structure.
4. Two Methyl Groups

Explanation

The compound contains two methyl (CH3) groups attached to the cyclopentane ring, which are responsible for its 1,4-dimethyl substitution.
5. Isopropyl Substitution

Explanation

The compound has an isopropyl (1-methylethyl) group attached to the cyclopentane ring at the 3-position.

Explanation

The stereochemistry of the compound is defined by the (1alpha,3alpha,4bta) configuration, which describes the spatial arrangement of the atoms in the molecule.
7. Synthetic Intermediate

Explanation

The compound is used as a synthetic intermediate, meaning it is a precursor in the synthesis of other, more complex molecules.
8. Chemical Building Block

Explanation

It serves as a chemical building block for the synthesis of various other compounds, making it a versatile starting material in organic chemistry.

Explanation

The compound may have potential applications in various industries, such as pharmaceuticals, agrochemicals, and materials science, due to its unique structure and properties.

Explanation

Further research may be needed to fully understand the compound's potential applications and to explore its specific chemical properties and uses.

Stereochemistry

(1alpha,3alpha,4bta)

Potential Applications

Pharmaceutical, Agrochemical, and Materials Industries

Further Research

Specific chemical properties and uses may vary

Check Digit Verification of cas no

The CAS Registry Mumber 189170-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,1,7 and 0 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 189170-44:
(8*1)+(7*8)+(6*9)+(5*1)+(4*7)+(3*0)+(2*4)+(1*4)=163
163 % 10 = 3
So 189170-44-3 is a valid CAS Registry Number.

189170-44-3Downstream Products

189170-44-3Relevant articles and documents

Sequenced Reactions with Samarium(II) Iodide. Domino Epoxide Ring-Opening/Ketyl Olefin Coupling Reactions

Molander, Gary A.,Losada, Carlos Del Pozo

, p. 2935 - 2943 (2007/10/03)

A new sequential reductive coupling process promoted by samarium(II) iodide is described. Cascade epoxide ring opening and ketyl radical olefin cyclization leads to a variety of cis-1,3-cyclopentanediols and cis-1,3-cyclohexanediols in good yields and with high diastereoselectivity.

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