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137105-99-8

Carbamic acid, [3-hydroxy-1-(hydroxymethyl)-2-methylpropyl]-, 1,1- 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, [3-hydroxy-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-

    Cas No: 137105-99-8

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  • 137105-99-8 Structure

  • Basic information

    1. Product Name: Carbamic acid, [3-hydroxy-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-
    2. Synonyms: Carbamic acid, [3-hydroxy-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-dimethylethyl ester, [S-(R*,R*)]- (9CI)
    3. CAS NO:137105-99-8
    4. Molecular Formula: C10H21NO4
    5. Molecular Weight: 219.27804
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 137105-99-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Carbamic acid, [3-hydroxy-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Carbamic acid, [3-hydroxy-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-(137105-99-8)
    11. EPA Substance Registry System: Carbamic acid, [3-hydroxy-1-(hydroxymethyl)-2-methylpropyl]-, 1,1-(137105-99-8)

  • 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: 137105-99-8(Hazardous Substances Data)

137105-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 137105-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,1,0 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 137105-99:
(8*1)+(7*3)+(6*7)+(5*1)+(4*0)+(3*5)+(2*9)+(1*9)=118
118 % 10 = 8
So 137105-99-8 is a valid CAS Registry Number.

137105-99-8Relevant articles and documents

Catalytic, asymmetric Mannich-type reactions of α-imino esters bearing readily removable substituents on nitrogen

Nakamura, Yoshitaka,Matsubara, Ryosuke,Kiyohara, Hiroshi,Kobayashi, Shu

, p. 2481 - 2484 (2007/10/03)

(Matrix presented) Catalytic, enantioselective Mannich-type reactions of α-imino esters bearing readily removable substituents on nitrogen are described. Several N-carbamate-protected α-imino esters, which are readily prepared from 2-bromoglycine esters using a polymer-supported amine, reacted with silicon enolates to afford the desired adducts in high yields with high enantioselectivity using a copper(II)-diamine complex. Easy deprotection of the product amine and transformation to free o-amino acid derivatives have also been demonstrated.

Isoindoline derivatives

-

, (2008/06/13)

Optically active 8-methoxyquinolonecarboxylic acids represented by the formula (I) wherein R1 is lower alkyl have been found to possess potent antibacterial activity against both Gram-negative and Gram-positive bacteria. The compounds may be synthesized from novel optically active intermediates.

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