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(3S,4R,5RS)-N-(4-methoxybenzyl)-3,4-bis(methoxymethyl)oxy-5-cyano-2-pyrrolidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 190902-21-7 Structure
  • Basic information

    1. Product Name: (3S,4R,5RS)-N-(4-methoxybenzyl)-3,4-bis(methoxymethyl)oxy-5-cyano-2-pyrrolidinone
    2. Synonyms:
    3. CAS NO:190902-21-7
    4. Molecular Formula:
    5. Molecular Weight: 350.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 190902-21-7.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: (3S,4R,5RS)-N-(4-methoxybenzyl)-3,4-bis(methoxymethyl)oxy-5-cyano-2-pyrrolidinone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S,4R,5RS)-N-(4-methoxybenzyl)-3,4-bis(methoxymethyl)oxy-5-cyano-2-pyrrolidinone(190902-21-7)
    11. EPA Substance Registry System: (3S,4R,5RS)-N-(4-methoxybenzyl)-3,4-bis(methoxymethyl)oxy-5-cyano-2-pyrrolidinone(190902-21-7)
  • 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: 190902-21-7(Hazardous Substances Data)

190902-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190902-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,9,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 190902-21:
(8*1)+(7*9)+(6*0)+(5*9)+(4*0)+(3*2)+(2*2)+(1*1)=127
127 % 10 = 7
So 190902-21-7 is a valid CAS Registry Number.

190902-21-7Downstream Products

190902-21-7Relevant articles and documents

Synthesis of nectrisine and related compounds, and their biological evaluation

Kim, Yong Jip,Takatsuki, Akira,Kogoshi, Naoto,Kitahara, Takeshi

, p. 8353 - 8364 (2007/10/03)

An efficient and novel process is described for the synthesis of nectrisine 5 and its related derivatives 6,7 as potent glucosidase inhibitors via the corresponding lactams starting from D-(-)-diethyl tartrate. Also the results of biological evaluation of the synthesized compounds are described.

Novel synthesis of nectrisine and 4-epi-nectrisine

Kim, Yong Jip,Kitahara, Takeshi

, p. 3423 - 3426 (2007/10/03)

Nectrisine 1, a potent glycosidase inhibitor, and 4-epi-Nectrisine 2 were synthesized from D-(-)-diethyl tartrate through the corresponding lactams. N-acyl protection was crucial to effect the reduction of the corresponding lactams to amino alcohols.

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