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CAS

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1444800-49-0

(1R,2S)‐2‐(((benzyloxy)imino)methyl)cyclopropane‐1‐carboxylic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1444800-49-0 Structure

  • Basic information

    1. Product Name: (1R,2S)‐2‐(((benzyloxy)imino)methyl)cyclopropane‐1‐carboxylic acid
    2. Synonyms: (1R,2S)‐2‐(((benzyloxy)imino)methyl)cyclopropane‐1‐carboxylic acid
    3. CAS NO:1444800-49-0
    4. Molecular Formula:
    5. Molecular Weight: 219.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1444800-49-0.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: (1R,2S)‐2‐(((benzyloxy)imino)methyl)cyclopropane‐1‐carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,2S)‐2‐(((benzyloxy)imino)methyl)cyclopropane‐1‐carboxylic acid(1444800-49-0)
    11. EPA Substance Registry System: (1R,2S)‐2‐(((benzyloxy)imino)methyl)cyclopropane‐1‐carboxylic acid(1444800-49-0)

  • 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: 1444800-49-0(Hazardous Substances Data)

1444800-49-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1444800-49-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,4,8,0 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1444800-49:
(9*1)+(8*4)+(7*4)+(6*4)+(5*8)+(4*0)+(3*0)+(2*4)+(1*9)=150
150 % 10 = 0
So 1444800-49-0 is a valid CAS Registry Number.

1444800-49-0Relevant articles and documents

Four Stereoisomers of 2-Aminomethyl-1-cyclopropanecarboxylic Acid: Synthesis and biological evaluation

Oikawa, Masato,Sugeno, Yuka,Tukada, Hideyuki,Takasaki, Yuichi,Takamizawa, Satoshi,Irie, Raku

, p. 1816 - 1823 (2019)

Here, we report a practical method for asymmetric synthesis of cyclopropane-fused GABA analogs. Starting from 2-furaldehyde, the cis-isomer (CAMP) was synthesized over 10 steps; (1)- and (+)-CAMP￠HCl were synthesized by employing d- and l-menth

A synthesis of (-)- cis -2-aminomethylcyclopropanecarboxylic acid [(-)-CAMP]

Oikawa, Masato,Sugeno, Yuka,Ishikawa, Yuichi,Tukada, Hideyuki

, p. 886 - 888 (2013/05/22)

An enantioselective synthesis of (-)-cis-2- aminomethylcyclopropanecarboxylic acid [(-)-CAMP] has been achieved in 2.5% total yield over ten steps starting from 2-furaldehyde. The synthesis features diastereoselective cyclopropane formation via diazene, followed by oxime formation and the reduction, for construction of the γ-aminobutyric acid (GABA) motif. Georg Thieme Verlag Stuttgart · New York.

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