2-Amino-6-hydroxybenzamide

Base Information

Chemical Name:2-Amino-6-hydroxybenzamide
CAS No.:136247-88-6
Molecular Formula:C7H8N2O2
Molecular Weight:152.15062
Hs Code.:
DSSTox Substance ID:DTXSID90568028
Nikkaji Number:J444.512K
Wikidata:Q82454149
Mol file:136247-88-6.mol

Synonyms:2-AMINO-6-HYDROXYBENZAMIDE;136247-88-6;Benzamide, 2-amino-6-hydroxy- (9CI);SCHEMBL2890578;DTXSID90568028;Benzamide,2-amino-6-hydroxy-(9ci);MB25426

Suppliers and Price of 2-Amino-6-hydroxybenzamide

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

Alichem
2-Amino-6-hydroxybenzamide
25g
$ 2626.40

Alichem
2-Amino-6-hydroxybenzamide
10g
$ 1608.00

Alichem
2-Amino-6-hydroxybenzamide
5g
$ 1290.42

Total 1 raw suppliers

Chemical Property of 2-Amino-6-hydroxybenzamide

Chemical Property:

PSA：90.33000
LogP:1.53870
XLogP3:0.9
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:152.058577502
Heavy Atom Count:11
Complexity:161

Purity/Quality:: 2-Amino-6-hydroxybenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C(=C1)O)C(=O)N)N

Technology Process of 2-Amino-6-hydroxybenzamide

There total 4 articles about 2-Amino-6-hydroxybenzamide 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:

: 1591-38-4
2-amino-6-methoxybenzamide

: 136247-88-6
6-hydroxyanthranilamide

Guidance literature:: With lithium methanethiolate; In N,N-dimethyl-formamide; at 80 ℃; for 6h; Yield given;
DOI:10.1021/jo00023a036

Reference yield:

: 60144-52-7
tert-butyl 3-methoxyphenylcarbamate

: 136247-88-6
6-hydroxyanthranilamide

Guidance literature:: Multi-step reaction with 3 steps

2: 95 percent / 6 N HCl / acetic acid / 2 h / Ambient temperature

3: LiSMe / dimethylformamide / 6 h / 80 °C

With hydrogenchloride; lithium methanethiolate; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jo00023a036

Reference yield:

: 536-90-3,918666-97-4
m-Anisidine

: 136247-88-6
6-hydroxyanthranilamide

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / tetrahydrofuran / 48 h / 50 °C

3: 95 percent / 6 N HCl / acetic acid / 2 h / Ambient temperature

4: LiSMe / dimethylformamide / 6 h / 80 °C

With hydrogenchloride; lithium methanethiolate; In tetrahydrofuran; acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jo00023a036