2H-1,3-Benzodioxole-5-carboximidamidium

Base Information

Chemical Name:2H-1,3-Benzodioxole-5-carboximidamidium
CAS No.:4720-71-2
Molecular Formula:C8H8 N2 O2
Molecular Weight:164.164
Hs Code.:2932999099
DSSTox Substance ID:DTXSID30963770
Wikidata:Q82945680
Mol file:4720-71-2.mol

Synonyms:DTXSID30963770;2H-1,3-Benzodioxole-5-carboximidamidium

Suppliers and Price of 2H-1,3-Benzodioxole-5-carboximidamidium

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

Labseeker
1,3-Benzodioxole-5-Carboximidamide 95
25g
$ 3245.00

Crysdot
Benzo[d][1,3]dioxole-5-carboximidamide 95+%
5g
$ 562.00

Chemenu
Benzo[1,3]dioxole-5-carboxamidine 95%
5g
$ 531.00

American Custom Chemicals Corporation
1,3-BENZODIOXOLE-5-CARBOXIMIDAMIDE 95.00%
5G
$ 2304.23

American Custom Chemicals Corporation
1,3-BENZODIOXOLE-5-CARBOXIMIDAMIDE 95.00%
2G
$ 1674.75

Alichem
Benzo[d][1,3]dioxole-5-carboximidamide
5g
$ 462.58

Total 15 raw suppliers

Chemical Property of 2H-1,3-Benzodioxole-5-carboximidamidium

Chemical Property:

Boiling Point:420.2 °C at 760 mmHg
Flash Point:207.9 °C
PSA：68.33000
LogP:1.49940
XLogP3:0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:165.066402534
Heavy Atom Count:12
Complexity:190

Purity/Quality:

97% ^*data from raw suppliers

1,3-Benzodioxole-5-Carboximidamide 95 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1OC2=C(O1)C=C(C=C2)C(=[NH2+])N

Technology Process of 2H-1,3-Benzodioxole-5-carboximidamidium

There total 2 articles about 2H-1,3-Benzodioxole-5-carboximidamidium 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:

: 60-29-7,927820-24-4
diethyl ether

: 61077-55-2
piperonal-((Z)-O-acetyl oxime )

: 4421-09-4
piperonylonitrile

: 20747-42-6
piperonal-(Z)-oxime

: 4720-71-2
benzo[d][1,3]dioxol-5-carboxyimidamide

Guidance literature:: Product distribution;
DOI:10.1021/jo01128a011

Reference yield:

: 61077-55-2
(E)-benzo[d][1,3]dioxole-5-carbaldehyde O-acetyl oxime

: 4421-09-4
piperonylonitrile

: 4720-71-2
benzo[d][1,3]dioxol-5-carboxyimidamide

Guidance literature:: With diethyl ether; ammonia; potassium amide; at -35 ℃; Behandeln des Reaktionsgemisches mit Ammoniumchlorid;
DOI:10.1021/jo01128a011

Reference yield: 41.0%

: 615-42-9
1,2-Diiodobenzene

: 4720-71-2
benzo[d][1,3]dioxol-5-carboxyimidamide

: 64499-60-1
N-phenylbenzo[1,3]dioxole-5-carboxamidine

: 2562-69-8
2-benzo[1,3]dioxol-5-yl-1H-benzoimidazole

Guidance literature:: With copper(l) iodide; caesium carbonate; N,N`-dimethylethylenediamine; In 1-methyl-pyrrolidin-2-one; at 170 ℃; Inert atmosphere;
DOI:10.1021/jo900912h