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Carbamic acid, (2,3-diaminopropyl)-, 1,1-dimethylethyl ester (9CI) 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-diaminopropyl)-, 1,1-dimethylethyl ester (9CI)

    Cas No: 163133-92-4

  • USD $ 1.9-2.9 / Gram

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  • 163133-92-4 Structure
  • Basic information

    1. Product Name: Carbamic acid, (2,3-diaminopropyl)-, 1,1-dimethylethyl ester (9CI)
    2. Synonyms: Carbamic acid, (2,3-diaminopropyl)-, 1,1-dimethylethyl ester (9CI);tert-butyl 2,3-diaminopropylcarbamate
    3. CAS NO:163133-92-4
    4. Molecular Formula: C8H19N3O2
    5. Molecular Weight: 189.25536
    6. EINECS: N/A
    7. Product Categories: N-BOC
    8. Mol File: 163133-92-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 331.9±32.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.047±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 12.34±0.46(Predicted)
    10. CAS DataBase Reference: Carbamic acid, (2,3-diaminopropyl)-, 1,1-dimethylethyl ester (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Carbamic acid, (2,3-diaminopropyl)-, 1,1-dimethylethyl ester (9CI)(163133-92-4)
    12. EPA Substance Registry System: Carbamic acid, (2,3-diaminopropyl)-, 1,1-dimethylethyl ester (9CI)(163133-92-4)
  • 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: 163133-92-4(Hazardous Substances Data)

163133-92-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 163133-92-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,1,3 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 163133-92:
(8*1)+(7*6)+(6*3)+(5*1)+(4*3)+(3*3)+(2*9)+(1*2)=114
114 % 10 = 4
So 163133-92-4 is a valid CAS Registry Number.

163133-92-4Downstream Products

163133-92-4Relevant articles and documents

Synthesis and properties of diazirinyl organo-platinum compounds for manipulations of photoaffinity labeled components

Hashimoto, Makoto,Furukawa, Keitaro,Tomohiro, Takenori,Hatanaka, Yasumaru

, p. 405 - 407 (2010)

Synthesis of diazirinyl organo-platinum complexes, which specifically interact with purine base, characterization of photoreactivity and interaction between guanosine 5′-monophosphate (GMP) were examined. The results indicated that the diazirinyl organo-platinum complex was useful for manipulations of photoaffinity labeled components.

Tricyclic erythromycin derivatives

-

, (2008/06/13)

Compounds, or pharmaceutically acceptable salts and esters thereof, of the formula: wherein A, B, D and E, R1, R2, and Z are specifically defined, having antibacterial activity, pharmaceutical compositions containing said compounds, treatment of bacterial infections with such compositions, and processes for the preparation of the compounds.

Convenient and simplified approaches to w-monoprotected triaminopropane derivatives: Key intermediates for bifunctional chelating agent synthesis

Benoist, Eric,Loussouarn, Anthony,Remaud, Patricia,Chatal, Jean-Francois,Gestin, Jean-Francois

, p. 1113 - 1118 (2007/10/03)

High yields of selectively Ar-protected-1,2,3-triaminopropanes (1,3 or 1,2 functionalized diamines) were obtained in 6 or 4 steps from diamino alcohols or aminodiols, respectively. These two multi-step procedures involve protection of the amino group, substitution of the hydroxy group by an azido group and selective reduction. The conditions for the first procedure allow the preparation of various Af2-monoprotected-l,2,3-triaminopropanes 6a, 6b, but the second one is more convenient for obtaining N1-Boc-1,2,3-triaminopropane 6'. These two simplified procedures, which provide functionalized 1,2 or 1,3 diamines easily and with good overall yields, could be useful for the synthesis of : bifunctional chelating agents.

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