Cas no 954238-88-1 ((2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER)

(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER structure
954238-88-1 structure
Product Name:(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER
CAS No:954238-88-1
MF:C11H15ClN2O2
MW:242.702001810074
MDL:MFCD09701245
CID:1985472
PubChem ID:84820093
Update Time:2024-10-25

(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER Chemical and Physical Properties

Names and Identifiers

    • (2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER
    • 1,1-Dimethylethyl N-(2-amino-5-chlorophenyl)carbamate (ACI)
    • tert-Butyl (2-amino-5-chlorophenyl)carbamate
    • G54982
    • EN300-1878549
    • SB40236
    • DB-257504
    • SCHEMBL15550749
    • tert-Butyl(2-amino-5-chlorophenyl)carbamate
    • CS-0342932
    • MFCD09701245
    • tert-butyl N-(2-amino-5-chlorophenyl)carbamate
    • 954238-88-1
    • MDL: MFCD09701245
    • Inchi: 1S/C11H15ClN2O2/c1-11(2,3)16-10(15)14-9-6-7(12)4-5-8(9)13/h4-6H,13H2,1-3H3,(H,14,15)
    • InChI Key: NMAXYAHHCCNXNL-UHFFFAOYSA-N
    • SMILES: O=C(NC1C(N)=CC=C(Cl)C=1)OC(C)(C)C

Computed Properties

  • Exact Mass: 242.0822054g/mol
  • Monoisotopic Mass: 242.0822054g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 4
  • Complexity: 253
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.3
  • Topological Polar Surface Area: 64.4?2

(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER Pricemore >>

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(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Sodium bicarbonate ,  Sodium dithionite Solvents: 1,4-Dioxane ,  Water ;  40 min, 100 °C
Reference
Discovery of a Selective Aurora A Kinase Inhibitor by Virtual Screening
Kilchmann, Falco; Marcaida, Maria J.; Kotak, Sachin; Schick, Thomas; Boss, Silvan D.; et al, Journal of Medicinal Chemistry, 2016, 59(15), 7188-7211

Production Method 2

Reaction Conditions
1.1 Catalysts: Guanidine hydrochloride Solvents: Ethanol ;  5 - 20 min, 35 - 40 °C
Reference
BF3·OEt2 Mediated metal-free one-pot sequential multiple annulation cascade (SMAC) synthesis of complex and diverse tetrahydroisoquinoline fused hybrid molecules
Shinde, Anand H.; Vidyacharan, Shinde; Sharada, Duddu S., Organic & Biomolecular Chemistry, 2016, 14(12), 3207-3211

(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER Raw materials

(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER Preparation Products

(2-AMINO-5-CHLORO-PHENYL)-CARBAMIC ACID TERT-BUTYL ESTER Related Literature

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