5-(Bromomethyl)-2,1,3-benzoxadiazole

Base Information

Chemical Name:5-(Bromomethyl)-2,1,3-benzoxadiazole
CAS No.:32863-31-3
Molecular Formula:C7H5BrN2O
Molecular Weight:213.033
Hs Code.:2934999090
European Community (EC) Number:670-651-9
DSSTox Substance ID:DTXSID60370812
Nikkaji Number:J1.704.204A
Wikidata:Q72446833
Mol file:32863-31-3.mol

Synonyms:32863-31-3;5-(bromomethyl)-2,1,3-benzoxadiazole;5-(bromomethyl)benzo[c][1,2,5]oxadiazole;5-Bromomethylbenzofurazan;5-Bromomethyl-2,1,3-benzoxadiazole;5-(bromomethyl)benzo [c][1,2,5]oxadiazole;2,1,3-Benzoxadiazole, 5-(bromomethyl)-;5-bromomethylbenzofurazane;5-(bromomethyl)benzofurazan;SCHEMBL243150;5-(bromomethyl)benzo[c]furazan;DTXSID60370812;BUJFLTNYWUEROF-UHFFFAOYSA-N;MFCD00174369;AKOS000265418;5-Bromomethyl-benzo[1,2,5]oxadiazole;AM85728;5-(bromomethyl)-2,1,3-benzooxadiazole;5-(Bromomethyl)benzo[2,1,3]oxadiazole;AC-26454;PS-10019;5-bromomethyl-benzo[c][1,2,5]oxadiazole;5-(bromomethyl)benzo[c]-[1,2,5]oxadiazole;FT-0619694;A26193;EN300-218154;F75516;J-516298;F0001-0973

Suppliers and Price of 5-(Bromomethyl)-2,1,3-benzoxadiazole

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
5-(Bromomethyl)-2,1,3-benzoxadiazole
100mg
$ 45.00

SynQuest Laboratories
5-(Bromomethyl)benzofurazan 97%
100 mg
$ 32.00

SynQuest Laboratories
5-(Bromomethyl)benzofurazan 97%
1 g
$ 144.00

Matrix Scientific
5-(Bromomethyl)-2,1,3-benzoxadiazole 95%
1g
$ 139.00

Matrix Scientific
5-(Bromomethyl)-2,1,3-benzoxadiazole 95%
10g
$ 924.00

Crysdot
5-(Bromomethyl)benzo[c][1,2,5]oxadiazole 95+%
10g
$ 338.00

Chemenu
5-(Bromomethyl)-2,1,3-benzoxadiazole 95%
10g
$ 319.00

Atlantic Research Chemicals
5-(Bromomethyl)-2,1,3-benzoxadiazole 95%
Price $/5gm:
$ 184.20

Atlantic Research Chemicals
5-(Bromomethyl)-2,1,3-benzoxadiazole 95%
Price $/1gm:
$ 47.64

Atlantic Research Chemicals
5-(Bromomethyl)-2,1,3-benzoxadiazole 95%
Price $/250mgs:
$ 22.23

Total 35 raw suppliers

Chemical Property of 5-(Bromomethyl)-2,1,3-benzoxadiazole

Chemical Property:

Vapor Pressure:0.00538mmHg at 25°C
Melting Point:77-80 °C
Refractive Index:1.661
Boiling Point:283.5 °C at 760 mmHg
PKA:-1.19±0.36(Predicted)
Flash Point:125.3 °C
PSA：38.92000
Density:1.742 g/cm³
LogP:2.11770
Storage Temp.:2-8°C
XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:211.95853
Heavy Atom Count:11
Complexity:144

Purity/Quality:

99%, ^*data from raw suppliers

5-(Bromomethyl)-2,1,3-benzoxadiazole ^*data from reagent suppliers

Safty Information:

Pictogram(s): C
Hazard Codes:C
Statements: 34
Safety Statements: 26-36/37/39-45

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=NON=C2C=C1CBr
Uses 5-(Bromomethyl)-2,1,3-benzoxadiazole is a useful research chemical.

Technology Process of 5-(Bromomethyl)-2,1,3-benzoxadiazole

There total 11 articles about 5-(Bromomethyl)-2,1,3-benzoxadiazole 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: 73.0%

: 20304-86-3
5-methyl-benzo[1,2,5]oxadiazole

: 32863-31-3
5-(bromomethyl)benzofurazan

Guidance literature:: With N-Bromosuccinimide; Perbenzoic acid; In tetrachloromethane; for 6h; Heating;

Reference yield: 60.0%

: 59660-56-9
benzo[c][1,2,5]oxadiazol-5-ylmethanol

: 32863-31-3
5-(bromomethyl)benzofurazan

Guidance literature:: With carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 4h; Cooling with ice;

Reference yield:

: 42564-51-2
4-fluoro-3-nitrobenzaldehyde

: 32863-31-3
5-(bromomethyl)benzofurazan

Guidance literature:: Multi-step reaction with 5 steps

1: sodium azide / dimethyl sulfoxide / 1 h

2: toluene / 5 h / 110 °C

3: triphenylphosphine / ethanol / 1 h / 70 °C

4: sodium tetrahydroborate; methanol / tetrahydrofuran / 1 h / Cooling with ice

5: triphenylphosphine; carbon tetrabromide / tetrahydrofuran / 4 h / 20 °C / Cooling with ice

With methanol; sodium tetrahydroborate; sodium azide; carbon tetrabromide; triphenylphosphine; In tetrahydrofuran; ethanol; dimethyl sulfoxide; toluene;