5-Chloro-2-methoxybenzenecarboximidamide

Base Information

Chemical Name:5-Chloro-2-methoxybenzenecarboximidamide
CAS No.:164670-74-0
Molecular Formula:C8H9ClN2O
Molecular Weight:184.625
Hs Code.:2925290090
DSSTox Substance ID:DTXSID00437150
Wikidata:Q82252536
Mol file:164670-74-0.mol

Synonyms:164670-74-0;5-Chloro-2-methoxybenzenecarboximidamide;5-Chloro-2-methoxybenzimidamide;5-Chloro-2-methoxy-benzamidine;SCHEMBL3911579;DTXSID00437150;WRYVNSLKWKHAGZ-UHFFFAOYSA-N;AKOS011783773;5-chloro-2-methoxybenzene-1-carboximidamide;CS-0302310;F83569;EN300-1966169;A919763

Suppliers and Price of 5-Chloro-2-methoxybenzenecarboximidamide

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

Matrix Scientific
5-Chloro-2-methoxybenzenecarboximidamide 97%
1g
$ 360.00

Crysdot
5-Chloro-2-methoxybenzimidamide 95+%
5g
$ 749.00

Atlantic Research Chemicals
5-Chloro-2-methoxybenzenecarboximidamide 95%
1gm:
$ 137.85

American Custom Chemicals Corporation
5-CHLORO-2-METHOXYBENZAMIDINE 95.00%
5MG
$ 495.11

AK Scientific
5-Chloro-2-methoxybenzenecarboximidamide
1g
$ 536.00

Total 3 raw suppliers

Chemical Property of 5-Chloro-2-methoxybenzenecarboximidamide

Chemical Property:

PSA：59.10000
LogP:2.43270
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:184.0403406
Heavy Atom Count:12
Complexity:174

Purity/Quality:

97% ^*data from raw suppliers

5-Chloro-2-methoxybenzenecarboximidamide 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)Cl)C(=N)N

Technology Process of 5-Chloro-2-methoxybenzenecarboximidamide

There total 4 articles about 5-Chloro-2-methoxybenzenecarboximidamide 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: 48.0%

: 55877-79-7
2-methoxy-5-chlorobenzonitrile

: 164670-74-0
5-chloro-2-methoxybenzimidamide

Guidance literature:: With lithium hexamethyldisilazane; In hexane; for 2h; Ambient temperature;
DOI:10.1021/jm00012a026

Reference yield:

: 7035-09-8
5-chloro-2-methoxybenzaldehyde

: 164670-74-0
5-chloro-2-methoxybenzimidamide

Guidance literature:: Multi-step reaction with 2 steps

1: 9.7 g / NH₄OH*HCl, NaOAc / formic acid / 4 h / Heating

2: 48 percent / lithium hexamethyldisilazane / hexane / 2 h / Ambient temperature

With sodium acetate; ammonium chloride; lithium hexamethyldisilazane; In formic acid; hexane;
DOI:10.1021/jm00012a026

Reference yield:

: 635-93-8
5-chlorosalicyclaldehyde

: 164670-74-0
5-chloro-2-methoxybenzimidamide

Guidance literature:: Multi-step reaction with 3 steps

1: 10 g / K₂CO₃ / dimethylformamide / 12 h / 60 °C

2: 9.7 g / NH₄OH*HCl, NaOAc / formic acid / 4 h / Heating

3: 48 percent / lithium hexamethyldisilazane / hexane / 2 h / Ambient temperature

With sodium acetate; potassium carbonate; ammonium chloride; lithium hexamethyldisilazane; In formic acid; hexane; N,N-dimethyl-formamide;
DOI:10.1021/jm00012a026