Dopachrome

Base Information

Chemical Name:Dopachrome
CAS No.:3571-34-4
Molecular Formula:C₉H₇NO₄
Molecular Weight:193.159
Hs Code.:
UNII:DWA58A6ZW7
DSSTox Substance ID:DTXSID30897147,DTXSID101205460
Nikkaji Number:J1.127.045J,J227.457D
Wikipedia:Dopachrome
Wikidata:Q5297282
Mol file:3571-34-4.mol

Synonyms:dopachrome

Suppliers and Price of Dopachrome

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

Total 4 raw suppliers

Chemical Property of Dopachrome

Chemical Property:

Vapor Pressure:1.41E-10mmHg at 25°C
Boiling Point:481.1°Cat760mmHg
PKA:1.97±0.20(Predicted)
Flash Point:244.8°C
PSA：83.47000
Density:1.56g/cm³
LogP:-0.27620
XLogP3:-0.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:193.03750770
Heavy Atom Count:14
Complexity:405

Purity/Quality:: 95%+ or 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1C(NC2=CC(=O)C(=O)C=C21)C(=O)O
Uses Dopachrome is a cyclized product of L-DOPA (D533751) and also the intermediate in the biosynthesis of melanin.

Technology Process of Dopachrome

There total 4 articles about Dopachrome 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:

: 60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine

: 89762-39-0,3571-34-4
dopachrome

: 59-92-7,90638-38-3
levodopa

Guidance literature:: With mushroom tyrosinase immobilized on silica; at 25 ℃; pH=6.8; Temperature; Kinetics; ammonium formate buffer; Continuous-flow bioreactor; Enzymatic reaction;
DOI:10.1002/rcm.5268

Reference yield:

: 60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine

: 3131-52-0
1H-indole-5,6-diol

: 59-92-7,90638-38-3
levodopa

: 18766-67-1
leucodopachromene

: 3571-34-4,89762-39-0
(2S)-dopachrome

Guidance literature:: With water; mushroom tyrosinase; Rate constant; phosphat buffer, ph 6.8;
DOI:10.1248/cpb.30.2094

Reference yield:

: 59-92-7,90638-38-3
levodopa

: 3131-52-0
1H-indole-5,6-diol

: 4790-08-3
5,6-dihydroxy-2-carboxyindole

: 89762-39-0,3571-34-4
dopachrome

Guidance literature:: With potassium hydroxide; sulfuric acid; oxygen; In water; at 25 ℃; for 0.666667h; pH=5.5; Product distribution / selectivity; Enzymatic reaction;