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148638-80-6

N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Carbamic acid, (2,3-dihydroxypropyl)(phenylmethyl)-, 1,1-dimethylethyl ester, (S)-

    Cas No: 148638-80-6

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  • 148638-80-6 Structure

  • Basic information

    1. Product Name: N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine
    2. Synonyms: N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine
    3. CAS NO:148638-80-6
    4. Molecular Formula:
    5. Molecular Weight: 281.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148638-80-6.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: N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine(148638-80-6)
    11. EPA Substance Registry System: N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine(148638-80-6)

  • 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: 148638-80-6(Hazardous Substances Data)

148638-80-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148638-80-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,6,3 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 148638-80:
(8*1)+(7*4)+(6*8)+(5*6)+(4*3)+(3*8)+(2*8)+(1*0)=166
166 % 10 = 6
So 148638-80-6 is a valid CAS Registry Number.

148638-80-6Relevant articles and documents

A straightforward synthesis of L-isoserinal

Junquera, Federico,Merchan, Francisco L.,Merino, Pedro,Tejero, Tomas

, p. 7045 - 7052 (2007/10/03)

A convenient preparation of L-isoserinal 3 in six steps and 32.8% overall yield employing D-glyceraldehyde acetonide I as starting material is described. The procedure is inexpensive, easily scaled up and proceeds without observable racemization.

FACILE SYNTHESIS OF OPTICALLY ACTIVE SULFONATES OF 4-tert-BUTOXYCARBONYL-2-HYDROXYMETHYLMORPHOLINE

Yanagisawa, Hiroaki,Kanazaki, Takuro

, p. 105 - 109 (2007/10/02)

Optically active sulfonates of 4-tert-butoxycarbonyl-2-hydroxymethylmorpholine were prepared from 1,2:5,6-di-O-D-mannitol by practical procedures.These compounds are versatile intermediates for optically active isomers of a number of neuropharmacologicall

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