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474302-74-4

trans-(1S,3R)-(-)-2-benzyl-3-ethoxycarbonyl-7-methoxy-1-methoxycarbonylethyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 474302-74-4 Structure

  • Basic information

    1. Product Name: trans-(1S,3R)-(-)-2-benzyl-3-ethoxycarbonyl-7-methoxy-1-methoxycarbonylethyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole
    2. Synonyms: trans-(1S,3R)-(-)-2-benzyl-3-ethoxycarbonyl-7-methoxy-1-methoxycarbonylethyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole
    3. CAS NO:474302-74-4
    4. Molecular Formula:
    5. Molecular Weight: 464.561
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 474302-74-4.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: trans-(1S,3R)-(-)-2-benzyl-3-ethoxycarbonyl-7-methoxy-1-methoxycarbonylethyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-(1S,3R)-(-)-2-benzyl-3-ethoxycarbonyl-7-methoxy-1-methoxycarbonylethyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole(474302-74-4)
    11. EPA Substance Registry System: trans-(1S,3R)-(-)-2-benzyl-3-ethoxycarbonyl-7-methoxy-1-methoxycarbonylethyl-9-methyl-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indole(474302-74-4)

  • 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: 474302-74-4(Hazardous Substances Data)

474302-74-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 474302-74-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,3,0 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 474302-74:
(8*4)+(7*7)+(6*4)+(5*3)+(4*0)+(3*2)+(2*7)+(1*4)=144
144 % 10 = 4
So 474302-74-4 is a valid CAS Registry Number.

474302-74-4Relevant articles and documents

Conformational analysis of the cis- and trans-adducts of the Pictet-Spengler reaction. Evidence for the structural basis for the C(1)-N(2) scission process in the cis- to trans-isomerization

Han, Dongmei,Foersterling, F. Holger,Deschamps, Jeffrey R.,Parrish, Damon,Liu, Xiaoxiang,Yin, Wenyuan,Huang, Shengming,Cook, James M.

, p. 75 - 82 (2008/03/31)

The stable conformations of both the trans- and cis-1,3-disubstituted Nb-benzyl stereoisomers of the Pictet-Spengler reaction have been determined by NMR spectroscopy and X-ray crystallography in order to better understand the C(1)-N(2) cis- to

A general strategy for the synthesis of vincamajine-related indole alkaloids: Stereocontrolled total synthesis of (+)-dehydrovoachalotine, (-)-vincamajinine, and (-)-11-methoxy-17-epivincamajine as well as the related quebrachidine diol, vincamajine diol,

Yu, Jianming,Wearing, Xiangyu Z.,Cook, James M.

, p. 3963 - 3979 (2007/10/03)

The highly convergent stereocontrolled total synthesis of (-)-vincamajinine (7), (-)-11-methoxy-17-epivincamajine (9), and the oxygen-bridged (+)-dehydrovoachalotine (22) are described. Key steps in the synthesis of 7 and 9 involved the stereospecific eno

Regiospecific, enantiospecific total synthesis of the alkoxy-substituted indole bases, 16-epi-Na-methylgardneral, 11-methoxyaffinisine, and 11-methoxymacroline as well as the indole alkaloids alstophylline and macralstonine

Liu, Xiaoxiang,Deschamp, Jeffrey R.,Cook, James M.

, p. 3339 - 3342 (2007/10/03)

(matrix presented) A regiospecific, enantiospecific approach to the synthesis of ring-A-substituted indole alkaloids was developed via a doubly convergent strategy. The asymmetric Pictet-Spengler reaction and enolate-driven palladium cross-coupling proces

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