L-ARG-7-AMINO-4-METHYLCOUMARIN

Base Information

Chemical Name:L-ARG-7-AMINO-4-METHYLCOUMARIN
CAS No.:70274-89-4
Molecular Formula:C₁₆H₂₁N₅O₃*2ClH
Molecular Weight:404.296
Hs Code.:
Mol file:70274-89-4.mol

Synonyms:

Suppliers and Price of L-ARG-7-AMINO-4-METHYLCOUMARIN

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

Chem-Impex
H-Arg-AMChydrochloridesalt
250MG
$ 477.57

Biosynth Carbosynth
H-Arg-AMC hydrochloride
1 g
$ 1750.00

Biosynth Carbosynth
H-Arg-AMC hydrochloride
500 mg
$ 1005.00

Biosynth Carbosynth
H-Arg-AMC hydrochloride
250 mg
$ 577.50

Biosynth Carbosynth
H-Arg-AMC hydrochloride
100 mg
$ 289.00

Biosynth Carbosynth
H-Arg-AMC hydrochloride
50 mg
$ 166.00

Total 10 raw suppliers

Chemical Property of L-ARG-7-AMINO-4-METHYLCOUMARIN

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

H-Arg-AMChydrochloridesalt ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of L-ARG-7-AMINO-4-METHYLCOUMARIN

There total 3 articles about L-ARG-7-AMINO-4-METHYLCOUMARIN 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: 97.0%

: Boc-Arg-AMC*HCl

: 69304-16-1,70274-89-4
H-Arg-AMC*2HCl

Guidance literature:: With hydrogenchloride; In diethyl ether; ethyl acetate; at 20 ℃;
DOI:10.1039/b906762k

Reference yield:

: 26093-31-2
7-amino-4-methylcoumarin.

: 69304-16-1,70274-89-4
H-Arg-AMC*2HCl

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; trichlorophosphate / -15 - 20 °C

2: hydrogenchloride / diethyl ether; ethyl acetate / 20 °C

With pyridine; hydrogenchloride; trichlorophosphate; In diethyl ether; ethyl acetate;
DOI:10.1039/b906762k

Reference yield:

: 13726-76-6,78603-12-0
t-butyloxycarbonyl-L-arginine

: 69304-16-1,70274-89-4
H-Arg-AMC*2HCl

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; trichlorophosphate / -15 - 20 °C

2: hydrogenchloride / diethyl ether; ethyl acetate / 20 °C

With pyridine; hydrogenchloride; trichlorophosphate; In diethyl ether; ethyl acetate;
DOI:10.1039/b906762k