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CHEMBRDG-BB 4011734

Base Information
  • Chemical Name:CHEMBRDG-BB 4011734
  • CAS No.:117654-86-1
  • Molecular Formula:C16H25NO3
  • Molecular Weight:279.379
  • Hs Code.:2924299090
  • Mol file:117654-86-1.mol
CHEMBRDG-BB 4011734

Synonyms:

Suppliers and Price of CHEMBRDG-BB 4011734
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
  • TRC
  • tert-ButylBenzyl(4-hydroxybutyl)carbamate
  • 500mg
  • $ 75.00
  • TRC
  • tert-ButylBenzyl(4-hydroxybutyl)carbamate
  • 100mg
  • $ 60.00
  • ChemBridge Corporation
  • tert-butylbenzyl(4-hydroxybutyl)carbamate 95%
  • 25 g
  • $ 356.00
  • American Custom Chemicals Corporation
  • TERT-BUTYL BENZYL(4-HYDROXYBUTYL)CARBAMATE 95.00%
  • 10G
  • $ 1679.66
  • American Custom Chemicals Corporation
  • TERT-BUTYL BENZYL(4-HYDROXYBUTYL)CARBAMATE 95.00%
  • 5G
  • $ 1138.78
  • American Custom Chemicals Corporation
  • TERT-BUTYL BENZYL(4-HYDROXYBUTYL)CARBAMATE 95.00%
  • 1G
  • $ 721.59
Total 3 raw suppliers
Chemical Property of CHEMBRDG-BB 4011734
Chemical Property:
  • Vapor Pressure:3.15E-07mmHg at 25°C 
  • Boiling Point:403.3oC at 760 mmHg 
  • Flash Point:197.7oC 
  • PSA:49.77000 
  • Density:1.063g/cm3 
  • LogP:3.19620 
Purity/Quality:

99.90% *data from raw suppliers

tert-ButylBenzyl(4-hydroxybutyl)carbamate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:
  • Statements: 25-43 
  • Safety Statements: 36/37-45 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of CHEMBRDG-BB 4011734

There total 10 articles about CHEMBRDG-BB 4011734 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:
4-(benzylamino)-1-butanol; With sodium hydroxide; tetrabutylammomium bromide; In dichloromethane; at 0 ℃; for 0.0833333h;
di-tert-butyl dicarbonate; In dichloromethane; at 0 - 20 ℃; for 6.5h;
Guidance literature:
Multi-step reaction with 2 steps
1: LiAlH4
2: triethylamine / CH2Cl2 / 20 °C
With lithium aluminium tetrahydride; triethylamine; In dichloromethane;
DOI:10.1021/ja051657t
Guidance literature:
Multi-step reaction with 3 steps
1: LiAlH4
2: triethylamine / CH2Cl2 / 20 °C
With lithium aluminium tetrahydride; triethylamine; In dichloromethane;
DOI:10.1021/ja051657t
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