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(1R,3S)-N-benzyl-3-(hydroxymethyl)-2,2-dimethylcyclopropanecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1199898-05-9 Structure
  • Basic information

    1. Product Name: (1R,3S)-N-benzyl-3-(hydroxymethyl)-2,2-dimethylcyclopropanecarboxamide
    2. Synonyms: (1R,3S)-N-benzyl-3-(hydroxymethyl)-2,2-dimethylcyclopropanecarboxamide
    3. CAS NO:1199898-05-9
    4. Molecular Formula:
    5. Molecular Weight: 233.31
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1199898-05-9.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,3S)-N-benzyl-3-(hydroxymethyl)-2,2-dimethylcyclopropanecarboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1R,3S)-N-benzyl-3-(hydroxymethyl)-2,2-dimethylcyclopropanecarboxamide(1199898-05-9)
    11. EPA Substance Registry System: (1R,3S)-N-benzyl-3-(hydroxymethyl)-2,2-dimethylcyclopropanecarboxamide(1199898-05-9)
  • 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: 1199898-05-9(Hazardous Substances Data)

1199898-05-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1199898-05-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,9,8,9 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1199898-05:
(9*1)+(8*1)+(7*9)+(6*9)+(5*8)+(4*9)+(3*8)+(2*0)+(1*5)=239
239 % 10 = 9
So 1199898-05-9 is a valid CAS Registry Number.

1199898-05-9Downstream Products

1199898-05-9Relevant articles and documents

Enantioselective synthesis of quaternary stereogenic centers through catalytic asymmetric addition of dimethylzinc to α-ketoesters with chiral cis-cyclopropane-based amide alcohol as ligand

Zheng, Bing,Hou, Shicong,Li, Zhiyuan,Guo, Hongchao,Zhong, Jiangchun,Wang, Min

, p. 2125 - 2129 (2009)

A new amino alcohol with a chiral cyclopropane backbone has been developed and used in the catalytic asymmetric diethylzinc addition to various types of α-ketoesters. This cyclopropane-based chiral amino alcohol shows moderate enantioselectivity in the ad

Preparation method of hydroxyamide

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Paragraph 0092-0095, (2020/02/10)

The invention discloses a preparation method of a hydroxyamide shown as formula (I). The hydroxyamide is prepared through homogeneous catalytic hydrogenation reaction of a cyclic imide represented byformula (II), wherein R1, R2 and R3 are respectively and

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