CID 4380138

Base Information

Chemical Name:CID 4380138
CAS No.:1956-25-8
Molecular Formula:C18H18 N2 O3
Molecular Weight:310.353
Hs Code.:2933990090
Mol file:1956-25-8.mol

Synonyms:

Suppliers and Price of CID 4380138

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

TCI Chemical
5-Benzyloxy-DL-tryptophan >98.0%(T)
100mg
$ 128.00

Matrix Scientific
5-(Benzyloxy)tryptophan
500mg
$ 199.00

Crysdot
(S)-2-Amino-3-(5-(benzyloxy)-1H-indol-3-yl)propanoicacid 97%
1g
$ 335.00

Chemenu
(S)-2-Amino-3-(5-(benzyloxy)-1H-indol-3-yl)propanoicacid 97%
1g
$ 316.00

American Custom Chemicals Corporation
5-BENZYLOXYTRYPTOPHAN 95.00%
5MG
$ 498.33

American Custom Chemicals Corporation
5-BENZYLOXYTRYPTOPHAN 95.00%
1G
$ 738.00

AK Scientific
5-(Benzyloxy)tryptophan
500mg
$ 318.00

Activate Scientific
5-Benzyloxy-DL-tryptophan 95%
1 g
$ 804.00

Acrotein
5-Benzyloxy-DL-tryptophan 97%
1g
$ 660.00

Acrotein
5-Benzyloxy-DL-tryptophan 97%
0.5g
$ 440.00

Total 18 raw suppliers

Chemical Property of CID 4380138

Chemical Property:

Vapor Pressure:1.56E-13mmHg at 25°C
Melting Point:275-276 °C (decomp)
Boiling Point:563.4°Cat760mmHg
PKA:2.22±0.10(Predicted)
Flash Point:294.6°C
PSA：88.34000
Density:1.323g/cm³
LogP:3.40160
XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:310.13174244
Heavy Atom Count:23
Complexity:392

Purity/Quality:

97% ^*data from raw suppliers

5-Benzyloxy-DL-tryptophan >98.0%(T) ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)COC2=CC3=C(C=C2)NC=C3CC(C(=O)[O-])[NH3+]

Technology Process of CID 4380138

There total 8 articles about CID 4380138 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:

: 1453-97-0
5-benzyloxygramine

: 1956-25-8
5-Benzyloxy-tryptophan

Guidance literature:: Multi-step reaction with 2 steps

1: NaOH; toluene

2: aqueous NaOH / anschliessend erwaermen mit wss. HCl

With sodium hydroxide; toluene;
DOI:10.1021/ja01651a001

Reference yield:

: (5-benzyloxy-indol-3-ylmethyl)-formylamino-malonic acid diethyl ester

: 1956-25-8
5-Benzyloxy-tryptophan

Guidance literature:: With sodium hydroxide; anschliessend erwaermen mit wss. HCl;
DOI:10.1021/ja01651a001

Reference yield:

: 1215-59-4
5-benzyloxy-1H-indole

: 1956-25-8
5-Benzyloxy-tryptophan

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid; dioxane

2: NaOH; toluene

3: aqueous NaOH / anschliessend erwaermen mit wss. HCl

With 1,4-dioxane; sodium hydroxide; acetic acid; toluene;
DOI:10.1021/ja01651a001