6-Ethylguanine

Base Information

Chemical Name:6-Ethylguanine
CAS No.:51866-19-4
Molecular Formula:C7H9 N5 O
Molecular Weight:179.181
Hs Code.:2933990090
NSC Number:37368
UNII:45T1754HHH
DSSTox Substance ID:DTXSID20199829
Nikkaji Number:J458.797I
Wikidata:Q83072832
ChEMBL ID:CHEMBL406419
Mol file:51866-19-4.mol

Synonyms:6-ethylguanine;O(6)-ethylguanine

Suppliers and Price of 6-Ethylguanine

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
6-EthylGuanine
1g
$ 165.00

Crysdot
6-Ethoxy-9H-purin-2-amine 97%
1g
$ 559.00

Chemenu
6-Ethoxy-9H-purin-2-amine 97%
1g
$ 528.00

American Custom Chemicals Corporation
O6-ETHYLGUANINE 95.00%
5MG
$ 502.35

AccelPharmtech
6-ethoxy-9H-Purin-2-amine 97.00%
5G
$ 1700.00

Total 9 raw suppliers

Chemical Property of 6-Ethylguanine

Chemical Property:

Vapor Pressure:0.0011mmHg at 25°C
Boiling Point:569°Cat760mmHg
Flash Point:297.9°C
PSA：89.71000
Density:1.441g/cm³
LogP:0.91500
XLogP3:0.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:179.08070993
Heavy Atom Count:13
Complexity:178

Purity/Quality:

97% ^*data from raw suppliers

6-EthylGuanine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCOC1=NC(=NC2=C1NC=N2)N
Uses 6-Ethyl Guanine is a alkylated mutagen of Guanine (G836000), usually indicative of carcinoma if detected. Guanine is on one of the five nucleobases incorporated into biological nucleic acids.

Technology Process of 6-Ethylguanine

There total 1 articles about 6-Ethylguanine 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:

: 51866-19-4
NU₂₀₄₆

: 56287-17-3,69123-94-0,784-71-4
2'-deoxy-2'-fluorouridine

Guidance literature:

Reference yield: 37.0%

: 4330-21-6
2-deoxy-3,5-di-O-p-toluoyl-α-D-erythro-pentofuranosyl chloride

: 51866-19-4
NU₂₀₄₆

: 7-[2-deoxy-3,5-di-O-(4-toluoyl)-β-D-erythro-pentofuranosyl]-6-(ethoxy)-7H-purin-2-amine

: 9-[2-deoxy-3,5-di-O-(4-toluoyl)-β-D-erythro-pentafuranosyl]-6-ethoxy-9H-purin-2-amine

Guidance literature:: With potassium hydroxide; Tris(3,6-dioxaheptyl)amine; In acetonitrile; for 0.333333h; Ambient temperature;
DOI:10.1002/hlca.19970800424

Reference yield:

: 51866-19-4
NU₂₀₄₆

: 50704-46-6
2'-deoxy-O⁶-ethylguanosine

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / KOH, tris-<2-(2-methoxyethoxy)ethyl>amine / acetonitrile / 0.33 h / Ambient temperature

2: 79 percent / NaOMe / methanol / 0.5 h / Ambient temperature

With potassium hydroxide; Tris(3,6-dioxaheptyl)amine; sodium methylate; In methanol; acetonitrile;
DOI:10.1002/hlca.19970800424