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114624-39-4

abn-delta(8)-tetrahydrocannabinol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114624-39-4 Structure

  • Basic information

    1. Product Name: abn-delta(8)-tetrahydrocannabinol
    2. Synonyms: abn-delta(8)-tetrahydrocannabinol
    3. CAS NO:114624-39-4
    4. Molecular Formula: C17H22O2
    5. Molecular Weight: 258.35538
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114624-39-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 369.8°Cat760mmHg
    3. Flash Point: 153.9°C
    4. Appearance: /
    5. Density: 1.06g/cm3
    6. Vapor Pressure: 5.45E-06mmHg at 25°C
    7. Refractive Index: 1.543
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: abn-delta(8)-tetrahydrocannabinol(CAS DataBase Reference)
    11. NIST Chemistry Reference: abn-delta(8)-tetrahydrocannabinol(114624-39-4)
    12. EPA Substance Registry System: abn-delta(8)-tetrahydrocannabinol(114624-39-4)

  • 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: 114624-39-4(Hazardous Substances Data)

114624-39-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114624-39-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,6,2 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114624-39:
(8*1)+(7*1)+(6*4)+(5*6)+(4*2)+(3*4)+(2*3)+(1*9)=104
104 % 10 = 4
So 114624-39-4 is a valid CAS Registry Number.
InChI:InChI=1/C17H22O2/c1-10-5-6-14-13(7-10)16-11(2)8-12(18)9-15(16)19-17(14,3)4/h5,8-9,13-14,18H,6-7H2,1-4H3/t13-,14-/m1/s1

114624-39-4Downstream Products

114624-39-4Relevant articles and documents

Biomimetic Cannabinoid Synthesis Revisited: Batch and Flow All-Catalytic Synthesis of (±)-ortho-Tetrahydrocannabinols and Analogues from Natural Feedstocks

Giorgi, Pascal D.,Liautard, Virginie,Pucheault, Mathieu,Antoniotti, Sylvain

, p. 1307 - 1311 (2018/04/02)

Using a combination of Au nanoparticle-catalyzed oxidation under an O2 atmosphere and a Ti-doped montmorillonite (Ti-MMT)-catalyzed tandem arylation/double cyclization, we developed an original and highly selective method for the synthesis of ortho-tetrahydrocannabinol derivatives from simple substrates. The reaction sequence could be performed in two steps in batch mode or in a single operation in continuous-flow reactors. The abnormal regioselectivity was proposed to be the result of the non-innocent role of the MMT support, TiIV cation coordination, and a Lewis acid-assisted Br?nsted acid (LBA) mechanism.

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