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CAS

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168034-32-0

(S)-4-<(S)-1-(benzyloxy)ethyl>-3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 168034-32-0 Structure

  • Basic information

    1. Product Name: (S)-4-<(S)-1-(benzyloxy)ethyl>-3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidine
    2. Synonyms:
    3. CAS NO:168034-32-0
    4. Molecular Formula:
    5. Molecular Weight: 335.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 168034-32-0.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: (S)-4-<(S)-1-(benzyloxy)ethyl>-3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-4-<(S)-1-(benzyloxy)ethyl>-3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidine(168034-32-0)
    11. EPA Substance Registry System: (S)-4-<(S)-1-(benzyloxy)ethyl>-3-t-butoxycarbonyl-2,2-dimethyl-1,3-oxazolidine(168034-32-0)

  • 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: 168034-32-0(Hazardous Substances Data)

168034-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 168034-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,8,0,3 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 168034-32:
(8*1)+(7*6)+(6*8)+(5*0)+(4*3)+(3*4)+(2*3)+(1*2)=130
130 % 10 = 0
So 168034-32-0 is a valid CAS Registry Number.

168034-32-0Relevant articles and documents

Dehydrooligopeptides. XVII. Practical syntheses of all of the diastereomers of N,N-protected 2,3-diaminobutanoic acids from L- and D-threonine derivatives

Nakamura,Hirai,Tamotsu,Yonezawa,Shin

, p. 1369 - 1377 (2007/10/02)

Syntheses of all of the dioctereomers of 2,3-diaminobutanoic acids, found in some pedtide antibiotics and toxins, were accomplished. The four isomers were derived mainly through two pathways including S(N)2 inversions of the β-substituent of L- or D-threonine derivatives. The various protecting groups and effective nucleophiles for the S(N)2 inversion were examined.

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