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3-Cyclohexene-1,1-dimethanol, dibenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 194023-52-4 Structure
  • Basic information

    1. Product Name: 3-Cyclohexene-1,1-dimethanol, dibenzoate
    2. Synonyms:
    3. CAS NO:194023-52-4
    4. Molecular Formula: C22H22O4
    5. Molecular Weight: 350.414
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 194023-52-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-Cyclohexene-1,1-dimethanol, dibenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Cyclohexene-1,1-dimethanol, dibenzoate(194023-52-4)
    11. EPA Substance Registry System: 3-Cyclohexene-1,1-dimethanol, dibenzoate(194023-52-4)
  • 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: 194023-52-4(Hazardous Substances Data)

194023-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194023-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,0,2 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 194023-52:
(8*1)+(7*9)+(6*4)+(5*0)+(4*2)+(3*3)+(2*5)+(1*2)=124
124 % 10 = 4
So 194023-52-4 is a valid CAS Registry Number.

194023-52-4Relevant articles and documents

Two convergent approaches toward novel carbocyclic C-nucleosides

Nencka, Radim,Sala, Michal,Dejmek, Milan,Drainsky, Martin,Holy, Antonin,Hebabecky, Hubert

scheme or table, p. 4119 - 4130 (2011/02/22)

Two convergent methodologies for construction of novel carbocyclic C-nucleosides allowing the syntheses of derivatives with uracil heterobase substituted at the position C-5 as well as C-6 were developed. The crucial step of the first methodology was the

Novel non-nucleosidic phosphoramidites for oligonucleotide modification and labeling

Su, Sheng-Hui,Iyer, Rajkumar S.,Aggarwal, Sunil K.,Kalra, Krishan L.

, p. 1639 - 1644 (2007/10/03)

A series of novel labeled phosphoramidites and CPG supports 1a-f with a new non-nucleosidic backbone based upon cyclohexyl-4-amino-1,1-dimethanol have been synthesized. These reagents have been used to label oligonucleotides with biotin and fluorescein at the 5'-, the 3'-, and internal positions.

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