DIBENZ(b,f)(1,4)OXAZEPINE supplier

Name
Dibenz-(b,f)-1,4-oxazephine
EINECS
CAS No. 257-07-8
Article Data26
CAS DataBase
Density 1.16g/cm³
Solubility
Melting Point
Formula C13H9 N O
Boiling Point 329.3°Cat760mmHg
Molecular Weight 195.221
Flash Point 125°C
Transport Information
Appearance
Safety Poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion and inhalation. Experimental teratogenic and reproductive effects. A human skin and eye irritant. Questionable carcinogen with experimental carcinogenic and tumorigenic data. When heated to decomposition it emits toxic fumes of NO_x.
Risk Codes
Molecular Structure
Hazard Symbols
Synonyms CR; CR(lacrimator); NSC 293779
PSA 21.59000
LogP 2.97850

Synthetic route

: 446-52-6
2-Fluorobenzaldehyde

: 95-55-6
2-amino-phenol

A: 257-07-8
dibenz[b,f][1,4]oxazepine

B: 212758-52-6
2-(2-fluorophenyl)benzo[d]oxazole

Conditions

Conditions	Yield
With oxygen; 1,3-diethyl-1H-benzo[d]imidazol-3-ium bromide; sodium hydroxide In o-xylene; para-xylene; m-xylene at 120℃; for 10h; Molecular sieve; Green chemistry;	A 25% B 65%

...Expand

: 446-52-6
2-Fluorobenzaldehyde

: 95-55-6
2-amino-phenol

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With poly(ethylene glycol)-400; potassium carbonate at 100℃; for 8h; Product distribution; Further Variations:; Reagents; Solvents; Temperatures; time;	89%
Stage #1: 2-amino-phenol In polyethylene glycol (300) at 50℃; for 0.5h; Stage #2: 2-Fluorobenzaldehyde In polyethylene glycol (300) at 50℃; for 10h; Stage #3: With potassium carbonate In polyethylene glycol (300) at 100℃; for 10h;	80%
With potassium carbonate at 100℃; Sealed tube;	58%

: 6266-10-0
2-[(2-chlorobenzylidene)amino]phenol

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Stage #1: 2-[(2-chlorobenzylidene)amino]phenol With potassium hydroxide In methanol at 20℃; for 0.583333h; Stage #2: In dimethyl sulfoxide at 120℃; for 2h; Further stages.;	75%
Stage #1: 2-[(2-chlorobenzylidene)amino]phenol With potassium hydroxide In methanol at 20℃; for 1h; Stage #2: In dimethyl sulfoxide at 150℃; for 6h;
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 89-98-5
2-chloro-benzaldehyde

: 95-55-6
2-amino-phenol

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With potassium hydroxide In N,N-dimethyl-formamide at 120℃; for 0.1h; Temperature; Reagent/catalyst; Microwave irradiation;	87%
Stage #1: 2-chloro-benzaldehyde; 2-amino-phenol In 5,5-dimethyl-1,3-cyclohexadiene for 2h; Reflux; Stage #2: In 5,5-dimethyl-1,3-cyclohexadiene at 120℃; for 24h; Stage #3: With sodium In 5,5-dimethyl-1,3-cyclohexadiene for 6h; Reflux;	75%

: 536-74-3
phenylacetylene

: 95-55-6
2-amino-phenol

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With tetrabutylammonium acetate; palladium diacetate; 1,2-diamino-benzene In N,N-dimethyl-formamide at 120℃; Microwave irradiation;	82%

: 2770-12-9
N-(2-phenoxyphenyl)formamide

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With polyphosphiric acid; trichlorophosphate at 120 - 130℃; for 2h; Cyclization;	75%

: 2-formamido-4'-tert-butyldiphenyl ester

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With polyphosphiric acid; trichlorophosphate at 120 - 130℃; for 2h; Cyclization;	56%

: 100-52-7
benzaldehyde

: 95-55-6
2-amino-phenol

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With potassium carbonate at 100℃; for 5h;	68%

: 95-55-6
2-amino-phenol

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 2-formamido-4'-tert-butyldiphenyl ester

A: 257-07-8
dibenz[b,f][1,4]oxazepine

B: 2-tert-butyl-dibenzo[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With polyphosphiric acid; trichlorophosphate at 120 - 130℃; for 2h; Cyclization;	A 23% B 31%

: 446-52-6
2-Fluorobenzaldehyde

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme
Multi-step reaction with 3 steps 1: potassium tert-butylate / N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme
Multi-step reaction with 3 steps 1: sodium hydrogencarbonate / N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 66961-19-1
2-(2-nitrophenoxy)benzaldehyde

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With iron In methanol; water for 6h; Reflux;

: 72084-13-0
2-phenoxybenzamide

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With PPA at 120 - 130℃; Cyclization;

: C13H9FNO(1-)*K(1+)

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 140℃; Microwave irradiation;

: C13H9FNO(1-)*Na(1+)

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 140℃; Microwave irradiation;

: C13H10FNO

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 140℃; Microwave irradiation;

: C13H10ClNO

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 140℃; Microwave irradiation;

: C13H10BrNO

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 140℃; Microwave irradiation;

: C13H10INO

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
In N,N-dimethyl-formamide at 140℃; Microwave irradiation;

: 89-98-5
2-chloro-benzaldehyde

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 6630-33-7
ortho-bromobenzaldehyde

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 26260-02-6
2-iodobenzaldehyde

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 3: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: C13H9FNO(1-)*K(1+)

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: C13H9FNO(1-)*Na(1+)

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 2805-76-7
GRI 378898

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 36456-43-6
2-Hydroxy-N-<2-brom-benzyliden>-anilin

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 218280-60-5
C13H10INO

: 257-07-8
dibenz[b,f][1,4]oxazepine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: N,N-dimethyl-formamide / 140 °C / Microwave irradiation 2: N,N-dimethyl-formamide / 140 °C / Microwave irradiation View Scheme

: 72228-26-3
S-phenyl 2-diazoethanethiolate

: 257-07-8
dibenz[b,f][1,4]oxazepine

: (+/-)-trans-2-phenylthioazeto[1,2-d]dibenzo[b,f]oxazepin-1-one

Conditions

Conditions	Yield
In toluene at 80℃; for 1.5h; Staudinger reaction;	99%
In benzene at 80℃; for 1h;	99%

: 120-72-9
indole

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 2-(2-(di(1H-indol-3-yl)methyl)phenoxy)aniline

Conditions

Conditions	Yield
With trifluoroacetic acid In dichloromethane at 20℃; for 3h; Catalytic behavior; Solvent; Friedel-Crafts Alkylation;	99%

: 1215-59-4
5-benzyloxy-1H-indole

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 2-(2-(bis(5-(benzyloxy)-1H-indol-3-yl)methyl)phenoxy)aniline

Conditions

Conditions	Yield
With trifluoroacetic acid In dichloromethane at 20℃; for 3h; Friedel-Crafts Alkylation;	99%

: 933-67-5
7-methyl-1H-indole

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 2-(2-(bis(7-methyl-1H-indol-3-yl)methyl)phenoxy)aniline

Conditions

Conditions	Yield
With trifluoroacetic acid In dichloromethane at 20℃; for 3h; Friedel-Crafts Alkylation;	99%

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 3158-85-8
10H-dibenzo[b,f][1,4]oxazepin-11-one

Conditions

Conditions	Yield
With dipotassium peroxodisulfate In ethanol; N,N-dimethyl-formamide at 50℃; for 1h; Time; Reagent/catalyst;	98%

: 1006-94-6
5-methoxylindole

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 2-(2-(bis(5-methoxy-1H-indol-3-yl)methyl)phenoxy)aniline

Conditions

Conditions	Yield
With trifluoroacetic acid In dichloromethane at 20℃; for 1.5h; Friedel-Crafts Alkylation;	98%

: 1,5,7-trimethyl-3-diazooxindole

: 257-07-8
dibenz[b,f][1,4]oxazepine

: spiro[5,7-dimethyloxindole-imidazo-bis(tetrahydro-dibenzo[1,4]oxazepine)]

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In tetrahydrofuran at 15 - 20℃; for 24h; diastereoselective reaction;	93%

: 3265-14-3
3-diazo-1-methyl-1,3-dihydro-indol-2-one

: 257-07-8
dibenz[b,f][1,4]oxazepine

: spiro[1-methyloxindole-imidazo-bis(tetrahydro-dibenzo[1,4]oxazepine)]

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In tetrahydrofuran at 15 - 20℃; for 24h; diastereoselective reaction;	93%

: 3265-14-3
3-diazo-1-methyl-1,3-dihydro-indol-2-one

: 257-07-8
dibenz[b,f][1,4]oxazepine

: C35H25N3O3

Conditions

Conditions	Yield
With p-toluenesulfonic acid monohydrate In tetrahydrofuran at 20℃; for 24h; Reagent/catalyst; diastereoselective reaction;	93%

: 1416060-68-8
C10H9N3O

: 257-07-8
dibenz[b,f][1,4]oxazepine

: C36H27N3O3

Conditions

Conditions	Yield
In tetrahydrofuran at 20℃; for 24h; diastereoselective reaction;	93%

: 7677-24-9
trimethylsilyl cyanide

: 257-07-8
dibenz[b,f][1,4]oxazepine

: (R)-10,11-dihydrodibenzo[b,f][1,4]oxazepine-11-carbonitrile

Conditions

Conditions	Yield
With 1-[3,5-bis(trifluoromethyl)phenyl]-3-{(S)[(2S,4S,5R)-5-ethyl-1-aza-bicyclo[2.2.2]oct-2-yl]-(6-methoxy-4-quinolinyl)methyl}thiourea; 2,2,2-trifluoroethanol In 1,2-dichloro-ethane at 4℃; for 30h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; enantioselective reaction;	93%

: 931-49-7
1-ethenylcyclohexene

: 257-07-8
dibenz[b,f][1,4]oxazepine

: (R)-11-(cyclohexenylethynyl)-10,11-dihydrodibenzo[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With (S)-CPA; silver(I) acetate In 1,4-dioxane at 15℃; for 72h; enantioselective reaction;	92%

: 78-93-3
butanone

: 257-07-8
dibenz[b,f][1,4]oxazepine

: (R)-1-(10,11-dihydrodibenzo[b,f][1,4]oxazepin-11-yl)butan-2-one

Conditions

Conditions	Yield
With L-proline In N,N-dimethyl-formamide at 20℃; Molecular sieve; enantioselective reaction;	92%

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 461677-71-4
1-benzyl-3-diazo-1,3-dihydro-2H-indol-2-one

: spiro[1-benzyloxindole-imidazo-bis(tetrahydro-dibenzo[1,4]oxazepine)]

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In tetrahydrofuran at 15 - 20℃; for 24h; diastereoselective reaction;	92%

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 20352-79-8
1-benzoyl-3- diazoindolin-2-one

: spiro[1-benzoyloxindole-imidazo-bis(tetrahydro-dibenzo[1,4]oxazepine)]

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In tetrahydrofuran at 15 - 20℃; for 24h; diastereoselective reaction;	92%

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 461677-71-4
1-benzyl-3-diazo-1,3-dihydro-2H-indol-2-one

: C41H29N3O3

Conditions

Conditions	Yield
With p-toluenesulfonic acid monohydrate In diethyl ether at 20℃; for 24h; Reagent/catalyst; Solvent; diastereoselective reaction;	92%

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 20352-79-8
1-benzoyl-3- diazoindolin-2-one

: C41H27N3O4

Conditions

Conditions	Yield
In para-xylene at 20℃; for 24h; diastereoselective reaction;	92%

: 1006-94-6
5-methoxylindole

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 11-(5-methoxy-1H-indol-3-yl)-10,11-dihydrodibenzo[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With trifluoroacetic acid In tetrahydrofuran at 20℃; for 0.5h; Friedel-Crafts Alkylation;	91%

: 603-76-9
1-methylindole

: 257-07-8
dibenz[b,f][1,4]oxazepine

: 11-(1-methyl-1H-indol-3-yl)-10,11-dihydrodibenzo[b,f][1,4]oxazepine

Conditions

Conditions	Yield
With trifluoroacetic acid In tetrahydrofuran at 20℃; for 1.5h; Friedel-Crafts Alkylation;	91%

: 3265-29-0
3-diazo-indolin-2-one

: 257-07-8
dibenz[b,f][1,4]oxazepine

: spiro[oxindole-imidazo-bis(tetrahydro-dibenzo[1,4]oxazepine)]

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In tetrahydrofuran at 15 - 20℃; for 24h; Solvent; Temperature; Reagent/catalyst; diastereoselective reaction;	91%

: 1419184-25-0
tert-butyl 3-diazo-2-oxoindoline-1-carboxylate

: 257-07-8
dibenz[b,f][1,4]oxazepine

: spiro[tert-butyl-1-carboxylateoxindole-imidazo-bis(tetrahydro-dibenzo[1,4]oxazepine)]

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In tetrahydrofuran at 15 - 20℃; for 24h; diastereoselective reaction;	91%

DIBENZ(b,f)(1,4)OXAZEPINE Chemical Properties

Product Name: Dibenz(b,f)(1,4)oxazepine (CAS NO.257-07-8)

Molecular Formula: C₁₃H₉NO
Molecular Weight: 195.21666g/mol
Mol File: 257-07-8.mol
Boiling point: 329.3 °C at 760 mmHg
Flash Point: 125 °C
Density: 1.16 g/cm³
Surface Tension: 43.7 dyne/cm
Enthalpy of Vaporization: 54.91 kJ/mol
Vapour Pressure: 0.000342 mmHg at 25°C
XLogP3-AA: 2.6
H-Bond Donor: 0
H-Bond Acceptor: 2

DIBENZ(b,f)(1,4)OXAZEPINE Toxicity Data With Reference

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
guinea pig	LCLo	inhalation	1500mg/m3/2H (1500mg/m3)		Toxicology. Vol. 8, Pg. 347, 1977.
guinea pig	LD50	intraperitoneal	463mg/kg (463mg/kg)	BEHAVIORAL: MUSCLE WEAKNESS BEHAVIORAL: ATAXIA SKIN AND APPENDAGES (SKIN): HAIR: OTHER	Toxicology. Vol. 8, Pg. 347, 1977.
guinea pig	LD50	oral	629mg/kg (629mg/kg)	BEHAVIORAL: GENERAL ANESTHETIC BEHAVIORAL: ATAXIA BEHAVIORAL: COMA	Toxicology. Vol. 8, Pg. 347, 1977.
hamster	LCLo	inhalation	1850mg/m3/3H (1850mg/m3)		Toxicology. Vol. 8, Pg. 347, 1977.
mouse	LCLo	inhalation	1500mg/m3/2H (1500mg/m3)		Toxicology. Vol. 8, Pg. 347, 1977.
mouse	LD50	intraperitoneal	242mg/kg (242mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
mouse	LD50	intravenous	37200ug/kg (37.2mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
mouse	LD50	oral	770mg/kg (770mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
rabbit	LCLo	inhalation	1500mg/m3/2H (1500mg/m3)		Toxicology. Vol. 8, Pg. 347, 1977.
rabbit	LD50	intravenous	26mg/kg (26mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
rabbit	LD50	oral	1760mg/kg (1760mg/kg)	BEHAVIORAL: GENERAL ANESTHETIC BEHAVIORAL: COMA BEHAVIORAL: ATAXIA	Toxicology. Vol. 8, Pg. 347, 1977.
rabbit	LD50	skin	> 400mg/kg (400mg/kg)		Toxicology. Vol. 8, Pg. 347, 1977.
rat	LD50	intraperitoneal	164mg/kg (164mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
rat	LD50	intravenous	26mg/kg (26mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,
rat	LD50	oral	563mg/kg (563mg/kg)		Interagency Collaborative Group on Environmental Carcinogenesis, National Cancer Institute, Memorandum, June 17, 1974Vol. 17JUN1974,

DIBENZ(b,f)(1,4)OXAZEPINE Consensus Reports

Reported in EPA TSCA Inventory.

DIBENZ(b,f)(1,4)OXAZEPINE Safety Profile

Poison by intraperitoneal and intravenous routes. Moderately toxic by ingestion and inhalation. Experimental teratogenic and reproductive effects. A human skin and eye irritant. Questionable carcinogen with experimental carcinogenic and tumorigenic data. When heated to decomposition it emits toxic fumes of NO_x.

DIBENZ(b,f)(1,4)OXAZEPINE Specification

Dibenz(b,f)(1,4)oxazepine ,its CAS NO. is 257-07-8,the synonyms is Dibenz(b,f)(1,4)oxazepine ; Dibenzo(b,f)-1,4oxazepine ; Dibenz-1,4-oxazepine ; Ea-3547 .

Product Name

Dibenz-(b,f)-1,4-oxazephine

Synthetic route

DIBENZ(b,f)(1,4)OXAZEPINE Chemical Properties

DIBENZ(b,f)(1,4)OXAZEPINE Toxicity Data With Reference

DIBENZ(b,f)(1,4)OXAZEPINE Consensus Reports

DIBENZ(b,f)(1,4)OXAZEPINE Safety Profile

DIBENZ(b,f)(1,4)OXAZEPINE Specification

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