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3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID

Base Information
  • Chemical Name:3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID
  • CAS No.:676348-90-6
  • Molecular Formula:C12H23NO4
  • Molecular Weight:245.31500
  • Hs Code.:2924190090
  • Mol file:676348-90-6.mol
3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID

Synonyms:3-tert-Butoxycarbonylamino-heptanoic acid;N-tert-butoxycarbonyl 3-amino-heptanoic acid;AA140;

Suppliers and Price of 3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • SynQuest Laboratories
  • 3-tert-Butoxycarbonylaminoheptanoic acid
  • 1 g
  • $ 616.00
  • Apolloscientific
  • 3-tert-Butoxycarbonylamino-heptanoicacid
  • 1g
  • $ 559.00
  • American Custom Chemicals Corporation
  • 3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID 95.00%
  • 5MG
  • $ 495.59
Total 4 raw suppliers
Chemical Property of 3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID
Chemical Property:
  • Vapor Pressure:7.9E-07mmHg at 25°C 
  • Boiling Point:380.1oC at 760 mmHg 
  • PKA:4.45±0.10(Predicted) 
  • Flash Point:183.7oC 
  • PSA:75.63000 
  • Density:1.048g/cm3 
  • LogP:2.93550 
Purity/Quality:

98%Min *data from raw suppliers

3-tert-Butoxycarbonylaminoheptanoic acid *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn 
  • Statements: 22 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID

There total 4 articles about 3-TERT-BUTOXYCARBONYLAMINO-HEPTANOIC ACID which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; In tert-butyl alcohol; at 20 ℃; for 1h;
DOI:10.1002/chem.200401295
Guidance literature:
Multi-step reaction with 2 steps
1.1: O3 / CH2Cl2; methanol / 2 h / -78 °C
1.2: Me2S / CH2Cl2; methanol / 1 h / -78 - 20 °C
2.1: aq. NaClO2; NaH2PO4; 2-methyl-2-butene / 2-methyl-propan-2-ol / 1 h / 20 °C
With sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; ozone; In methanol; dichloromethane; tert-butyl alcohol;
DOI:10.1002/chem.200401295
Guidance literature:
Multi-step reaction with 3 steps
1.1: diethyl ether / 6 h / 20 °C
2.1: O3 / CH2Cl2; methanol / 2 h / -78 °C
2.2: Me2S / CH2Cl2; methanol / 1 h / -78 - 20 °C
3.1: aq. NaClO2; NaH2PO4; 2-methyl-2-butene / 2-methyl-propan-2-ol / 1 h / 20 °C
With sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; ozone; In methanol; diethyl ether; dichloromethane; tert-butyl alcohol;
DOI:10.1002/chem.200401295
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