tert-butyl benzyl(4-iodobutyl)carbamate

Base Information

Chemical Name:tert-butyl benzyl(4-iodobutyl)carbamate
CAS No.:400045-79-6
Molecular Formula:C16H24INO2
Molecular Weight:389.277
Hs Code.:2924299090

Synonyms:tert-butyl N-benzyl-N-(4-iodobutyl)carbamate;

Suppliers and Price of tert-butyl benzyl(4-iodobutyl)carbamate

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

Sigma-Aldrich
tert-Butyl benzyl(4-iodobutyl)carbamate Aldrich
1g
$ 83.50

ChemBridge Corporation
tert-Butyl benzyl(4-iodobutyl)carbamate 90%
25 g
$ 356.00

American Custom Chemicals Corporation
TERT-BUTYL BENZYL(4-IODOBUTYL)CARBAMATE 95.00%
10G
$ 1994.98

American Custom Chemicals Corporation
TERT-BUTYL BENZYL(4-IODOBUTYL)CARBAMATE 95.00%
5G
$ 1334.03

American Custom Chemicals Corporation
TERT-BUTYL BENZYL(4-IODOBUTYL)CARBAMATE 95.00%
1G
$ 764.03

Total 1 raw suppliers

Chemical Property of tert-butyl benzyl(4-iodobutyl)carbamate

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:417.596oC at 760 mmHg
PKA:-1.36±0.70(Predicted)
Flash Point:206.355oC
PSA：29.54000
Density:1.371g/cm3
LogP:4.63890

Purity/Quality:

99% ^*data from raw suppliers

tert-Butyl benzyl(4-iodobutyl)carbamate Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22-43
Safety Statements: 36/37

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of tert-butyl benzyl(4-iodobutyl)carbamate

There total 1 articles about tert-butyl benzyl(4-iodobutyl)carbamate 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:

Reference yield: 53.0%

: 117654-86-1
4-[N-(t-butoxycarbonyl)-N-[(phenyl)methyl]-amino]butan-1-ol

: 400045-79-6
N-benzyl-N-(t-butoxycarbonyl)-4-amino-1-iodobutane

Guidance literature:: With Carbonyldiimidazole; methyl iodide; In acetonitrile; at 20 ℃; for 4h; Heating / reflux;

Reference yield: 69.0%

: 400045-79-6
N-benzyl-N-(t-butoxycarbonyl)-4-amino-1-iodobutane

: 220926-98-7
tert-butyl benzyl(but-3-en-1yl)carbamate

Guidance literature:: With (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; [CoCl₂(dmgH)2(pyridine)]; potassium carbonate; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 16h; Inert atmosphere; Sealed tube; Irradiation;
DOI:10.1021/jacs.1c06768