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CAS

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136312-26-0

(1S)-1-(2,2-Dimethoxyethyl)-1,2,3,4-tetrahydro-β-carboline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 136312-26-0 Structure

  • Basic information

    1. Product Name: (1S)-1-(2,2-Dimethoxyethyl)-1,2,3,4-tetrahydro-β-carboline
    2. Synonyms: (1S)-1-(2,2-Dimethoxyethyl)-1,2,3,4-tetrahydro-β-carboline
    3. CAS NO:136312-26-0
    4. Molecular Formula:
    5. Molecular Weight: 260.336
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 136312-26-0.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: (1S)-1-(2,2-Dimethoxyethyl)-1,2,3,4-tetrahydro-β-carboline(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S)-1-(2,2-Dimethoxyethyl)-1,2,3,4-tetrahydro-β-carboline(136312-26-0)
    11. EPA Substance Registry System: (1S)-1-(2,2-Dimethoxyethyl)-1,2,3,4-tetrahydro-β-carboline(136312-26-0)

  • 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: 136312-26-0(Hazardous Substances Data)

136312-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136312-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,3,1 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136312-26:
(8*1)+(7*3)+(6*6)+(5*3)+(4*1)+(3*2)+(2*2)+(1*6)=100
100 % 10 = 0
So 136312-26-0 is a valid CAS Registry Number.

136312-26-0Downstream Products

136312-26-0Relevant articles and documents

Diasteroselective cyclizations with enantiopure malonaldehyde monocycloacetals

Bi, Lanrong,Zhao, Ming,Wang, Chao,Peng, Shiqi,Winterfeldt, Ekkehard

, p. 22 - 26 (2007/10/03)

The synthesis of a series of enantiopure malonaldehyde monocycloacetals is described. Treatment of 8b with L-tryptophan methyl ester, 5-methoxytryptamine, and tryptamine, respectively, in the Pictet-Spengler condensation gave the corresponding enantiomerically pure key precursors 1-3 and 17-21 in only two steps. Using a chiral amino-diol successfully realized the kinetic resolution of racemic carbolines 23 and 24.

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