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CAS

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1283722-21-3

(2R,3R)-N,N-diallyl-4-(benzyloxy)-3-hydroxy-2-methylbutanethioamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1283722-21-3 Structure

  • Basic information

    1. Product Name: (2R,3R)-N,N-diallyl-4-(benzyloxy)-3-hydroxy-2-methylbutanethioamide
    2. Synonyms: (2R,3R)-N,N-diallyl-4-(benzyloxy)-3-hydroxy-2-methylbutanethioamide
    3. CAS NO:1283722-21-3
    4. Molecular Formula:
    5. Molecular Weight: 319.468
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1283722-21-3.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: (2R,3R)-N,N-diallyl-4-(benzyloxy)-3-hydroxy-2-methylbutanethioamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R,3R)-N,N-diallyl-4-(benzyloxy)-3-hydroxy-2-methylbutanethioamide(1283722-21-3)
    11. EPA Substance Registry System: (2R,3R)-N,N-diallyl-4-(benzyloxy)-3-hydroxy-2-methylbutanethioamide(1283722-21-3)

  • 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: 1283722-21-3(Hazardous Substances Data)

1283722-21-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1283722-21-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,3,7,2 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1283722-21:
(9*1)+(8*2)+(7*8)+(6*3)+(5*7)+(4*2)+(3*2)+(2*2)+(1*1)=153
153 % 10 = 3
So 1283722-21-3 is a valid CAS Registry Number.

1283722-21-3Downstream Products

1283722-21-3Relevant articles and documents

Direct catalytic enantio- and diastereoselective aldol reaction of thioamides

Iwata, Mitsutaka,Yazaki, Ryo,Chen, I-Hon,Sureshkumar, Devarajulu,Kumagai, Naoya,Shibasaki, Masakatsu

, p. 5554 - 5560 (2011/05/14)

A direct catalytic asymmetric aldol reaction of thioamides using a soft Lewis acid/hard Bronsted base cooperative catalyst comprising (R,R)-Ph-BPE/[Cu(CH3CN)4]PF6/LiOAr is described. Exclusive enolate generation from thioa

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