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CAS

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444814-26-0

N-[(R)-α-methylbenzyl]aziridine-2(S)-diphenylmethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 444814-26-0 Structure

  • Basic information

    1. Product Name: N-[(R)-α-methylbenzyl]aziridine-2(S)-diphenylmethanol
    2. Synonyms: N-[(R)-α-methylbenzyl]aziridine-2(S)-diphenylmethanol
    3. CAS NO:444814-26-0
    4. Molecular Formula:
    5. Molecular Weight: 329.442
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 444814-26-0.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: N-[(R)-α-methylbenzyl]aziridine-2(S)-diphenylmethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-[(R)-α-methylbenzyl]aziridine-2(S)-diphenylmethanol(444814-26-0)
    11. EPA Substance Registry System: N-[(R)-α-methylbenzyl]aziridine-2(S)-diphenylmethanol(444814-26-0)

  • 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: 444814-26-0(Hazardous Substances Data)

444814-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 444814-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,4,8,1 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 444814-26:
(8*4)+(7*4)+(6*4)+(5*8)+(4*1)+(3*4)+(2*2)+(1*6)=150
150 % 10 = 0
So 444814-26-0 is a valid CAS Registry Number.

444814-26-0Relevant articles and documents

An efficient synthesis of N-Boc-D-diphenylalanine from a chiral azirdine-2-carboxylate

Chang, Jae-Won,Ha, Hyun-Joon,Park, Chan Sun,Kim, Min Sung,Lee, Won Koo

, p. 1143 - 1148 (2007/10/03)

N-Boc-D-diphenylalanine was prepared from a commercially available aziridine-2(S)-carboxylate through alkylation, regiospecific aziridine ring opening, and benzylic deoxygenation followed by oxidation in 57% overall yield.

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