2-NITROBENZYL ALCOHOL supplier

Name
2-Nitrobenzyl alcohol
EINECS 210-302-6
CAS No. 612-25-9
Article Data197
CAS DataBase
Density 1.33 g/cm³
Solubility Soluble in water 5000 mg/L 20 deg Celsius.
Melting Point 69-72 °C(lit.)
Formula C₇H₇NO₃
Boiling Point 270 °C at 760 mmHg
Molecular Weight 153.137
Flash Point 131.1 °C
Transport Information UN 2811 6.1/PG 3
Appearance white to light yellow crystal powder
Safety 22-24/25-45-36/37/39-26-16
Risk Codes 11-34
Molecular Structure
Hazard Symbols Xi, C, F
Synonyms Benzylalcohol, o-nitro- (6CI,7CI,8CI);2-Nitrobenzenemethanol;NSC 66512;o-(Hydroxymethyl)nitrobenzene;o-Nitrobenzyl alcohol;
PSA 66.05000
LogP 1.61030

Synthetic route

: 552-89-6
2-nitro-benzaldehyde

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With magnesium(II) perchlorate; polymer-bound NADH (2a) In acetonitrile; benzene at 80℃; for 120h; Further byproducts given;	100%
With boron trifluoride diethyl etherate In tetrahydrofuran at 0℃;	100%
With zirconium dioxide hydrate; isopropyl alcohol at 60℃; for 0.1h; Meerwein-Ponndorf-Verley Reduction;	100%

: 606-27-9
methyl 2-nitrobenzoate

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With sodium tetrahydroborate In 1,4-dioxane; water for 2h; Ambient temperature;	100%
With sodium tetrahydroborate; zinc phthalocyanine In PEG-400 at 100℃; for 10h;	97%
With zinc(II) tetrahydroborate; cyclohexene In tetrahydrofuran for 3h; Heating;	80%

: C28H24BN4O12(1-)*Na(1+)

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With water	100%

: 62673-13-6
o-Nitrobenzyloxytrimethylsilane

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With Oxone In methanol for 0.25h; Heating;	98%
With methanol; 1,3-disulfonic acid imidazolium hydrogen sulfate at 20℃; for 0.0833333h; Green chemistry;	98%
With tris[trinitratocerium(IV)] paraperiodate at 20℃; for 0.0166667h;	95%

: 552-16-9
ortho-nitrobenzoic acid

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
Stage #1: ortho-nitrobenzoic acid With 4-methyl-morpholine; 1,3,5-trichloro-2,4,6-triazine In 1,2-dimethoxyethane at 20℃; for 3h; Esterification; Stage #2: With sodium tetrahydroborate In water at 0℃; Reduction;	97%
Stage #1: ortho-nitrobenzoic acid With sodium aminodiboranate In tetrahydrofuran at 20℃; Stage #2: With water	92%
With pyridine; methanol; sodium tetrahydroborate; trifluoro-[1,3,5]triazine 1.) CH2Cl2, -20 to -010 deg C, 1 h, 2.) room temperature, 10-15 min; Yield given. Multistep reaction;
With lithium aluminium tetrahydride In diethyl ether at 0℃; for 2h;	85 % Turnov.
Multi-step reaction with 2 steps 1: thionyl chloride; N,N-dimethyl-formamide / dichloromethane / 20 °C 2: sodium tetrahydroborate / tetrahydrofuran; N,N-dimethyl-formamide / 0 - 20 °C View Scheme

: 18483-88-0
o-(NO2)C6H4CH2OTHP

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With bismuth(lll) trifluoromethanesulfonate In methanol for 0.0833333h; Heating;	97%
With tetra-N-butylammonium tribromide In methanol at 20℃; for 0.5h;	95%
With Oxone In methanol for 1h; Heating;	94%
With silica triflate In methanol for 0.166667h; Heating;	90%
With dihydrogen peroxide; vanadia In water; acetonitrile for 0.25h; Heating;	97 % Chromat.

: C13H4NO4F5

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With sodium tetrahydroborate In tetrahydrofuran at 20℃; for 2.5h;	95%

: 1058649-36-7
2-nitro-1-[(ethoxymethoxy)methyl]benzene

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
phosphotungstic acid In ethanol for 2h; Heating;	89%

: 1058649-34-5
C9H11NO4

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With niobium pentachloride In acetonitrile at 0 - 20℃; for 1h;	88%
phosphotungstic acid In ethanol for 2h; Heating;	86%

: 610-14-0
2-nitrobenzyl chloride

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With (1,4-diazabicyclo{2.2.2}-octane)zinc(II) tetrahydoborate In tetrahydrofuran for 0.08h; Ambient temperature;	87%
With sodium tetrahydroborate In tetrahydrofuran; N,N-dimethyl-formamide at 0 - 20℃;

: 3958-60-9
2-nitrophenylmethyl bromide

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With oxygen; eosin y In dimethyl sulfoxide at 25℃; for 12h; Irradiation;	85%
Multi-step reaction with 2 steps 1: 96 percent / CHCl3 / 24 h / 50 °C 2: 77 percent / H2O / 24 h / Heating; 0.01 mol sulfonium salt - 150 ml water View Scheme
Stage #1: 2-nitrophenylmethyl bromide With dihydrogen peroxide In chlorobenzene for 2.5h; Reflux; Stage #2: With potassium carbonate In chlorobenzene for 16h; Reflux;
With di(pyridin-2-yl)amine; sodium hydroxide In N,N-dimethyl-formamide
With tetrabutylammomium bromide; sodium carbonate at 75℃; for 7h;	18 g

: 612-23-7
2-nitrobenzyl chloride

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With sodium hydroxide; 2,2-dimethyl-5-hydroxymethyl-5-nitro-1,3-dioxane In methanol for 24h; Irradiation;	82%
With water; potassium carbonate
With water; calcium carbonate

: 552-89-6
2-nitro-benzaldehyde

A: 612-25-9
2-Nitrobenzyl alcohol

B: 42467-41-4
2,2'-(oxybis(methylene))bis(nitrobenzene)

Conditions

Conditions	Yield
With triethylsilane; trifluorormethanesulfonic acid In nitromethane at 20℃; for 0.0333333h;	A 22% B 78%

: 99366-72-0
o-nitrobenzyldimethylsulfonium bromide

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With water for 24h; Heating; 0.01 mol sulfonium salt - 150 ml water;	77%

: 88-72-2
1-methyl-2-nitrobenzene

A: 552-16-9
ortho-nitrobenzoic acid

B: 612-25-9
2-Nitrobenzyl alcohol

C: 552-89-6
2-nitro-benzaldehyde

Conditions

Conditions	Yield
With ozone; cobalt(II) acetate In acetic acid at 100℃; Kinetics; Product distribution; Further Variations:; Catalysts; Temperatures;	A 75.4% B n/a C n/a
With Coprinus sp. peroxidase; tartaric acid buffer; dihydrogen peroxide In water; acetone at 20℃; pH=5;
Stage #1: 1-methyl-2-nitrobenzene With oxygen; cobalt(II) acetate; 2-hydroxy-4,5,6,7-tetraphenylisoindoline-1,3-dione at 110℃; under 2250.23 Torr; Stage #2: With water; oxygen at 61℃; under 1500.15 Torr;

...Expand

: 73961-59-8
tert-Butyl-dimethyl-(2-nitro-benzyloxy)-silane

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With N-Bromosuccinimide In water; dimethyl sulfoxide for 17h; Ambient temperature;	74%

: C28H25N3O6S

A: 612-25-9
2-Nitrobenzyl alcohol

B: C21H22N2O3S

Conditions

Conditions	Yield
With sodium tetrahydroborate In methanol	A n/a B 62%

: 134361-00-5
3,3-dimethyl-2-butanone lithium enolate

: 552-89-6
2-nitro-benzaldehyde

A: 552-16-9
ortho-nitrobenzoic acid

B: 612-25-9
2-Nitrobenzyl alcohol

C: 1-hydroxy-4,4-dimethyl-1-(2-nitrophenyl)pentan-3-one

D: 103457-25-6
(E)-4,4-dimethyl-1-(2-nitrophenyl)pent-1-en-3-one

Conditions

Conditions	Yield
In neat (no solvent, solid phase) at 20℃; for 0.5h;	A n/a B n/a C 51% D 9%

...Expand

: 552-89-6
2-nitro-benzaldehyde

A: 62635-27-2
1,2-bis(2-nitrophenyl)ethane-1,2-diol

B: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With trimethylphosphine-d9 In tetrahydrofuran at 20℃; for 12h; Inert atmosphere;	A 39% B 17%

: 73961-59-8
tert-Butyl-dimethyl-(2-nitro-benzyloxy)-silane

A: 612-25-9
2-Nitrobenzyl alcohol

B: 552-89-6
2-nitro-benzaldehyde

Conditions

Conditions	Yield
With tetra-N-butylammonium tribromide In acetonitrile at 20℃; for 20h; Irradiation;	A 12% B 23%

: 88-72-2
1-methyl-2-nitrobenzene

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
durch elektrolytische Oxydation;
Multi-step reaction with 2 steps 1.1: 2,2'-azobis(2,4-dimethylvaleronitrile); bromine / chlorobenzene / 0.5 h / 45 °C 2.1: dihydrogen peroxide / chlorobenzene / 2.5 h / Reflux 2.2: 16 h / Reflux View Scheme
Multi-step reaction with 2 steps 1.1: 2,2'-azobis(isobutyronitrile) / 1,2-dichloro-ethane; water / 0.25 h / 65 °C 1.2: 3.5 h 1.3: 3 h 2.1: sodium carbonate; tetrabutylammomium bromide / 7 h / 75 °C View Scheme
Stage #1: 1-methyl-2-nitrobenzene With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) In tetrachloromethane at 20 - 80℃; for 3h; Stage #2: With potassium carbonate In methanol; water at 80℃;

: 555-31-7
aluminum isopropoxide

: 67-63-0
isopropyl alcohol

: 552-89-6
2-nitro-benzaldehyde

: 612-25-9
2-Nitrobenzyl alcohol

...Expand

: 67-56-1
methanol

: 56-23-5
tetrachloromethane

: 552-89-6
2-nitro-benzaldehyde

A: 552-16-9
ortho-nitrobenzoic acid

B: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
Disproportionierung;

...Expand

: 50-00-0
formaldehyd

: 552-89-6
2-nitro-benzaldehyde

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With sodium hydroxide at 50 - 60℃;

: 64-17-5
ethanol

: 555-75-9
aluminum ethoxide

: 552-89-6
2-nitro-benzaldehyde

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
at 30℃;

...Expand

: 555-75-9
aluminum ethoxide

: 552-89-6
2-nitro-benzaldehyde

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With ethanol at 30℃;
With benzene bei Siedetemperatur;

: 555-31-7
aluminum isopropoxide

: 552-89-6
2-nitro-benzaldehyde

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With isopropyl alcohol

: 2269-22-9
aluminum tri-sec-butoxide

: 552-89-6
2-nitro-benzaldehyde

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
With iso-butanol

: 2269-22-9
aluminum tri-sec-butoxide

: 552-89-6
2-nitro-benzaldehyde

: 78-92-2, 15892-23-6
iso-butanol

: 612-25-9
2-Nitrobenzyl alcohol

...Expand

: 555-75-9
aluminum ethoxide

: 552-89-6
2-nitro-benzaldehyde

: 71-43-2
benzene

: 612-25-9
2-Nitrobenzyl alcohol

Conditions

Conditions	Yield
bei Siedetemperatur;

...Expand

: 612-25-9
2-Nitrobenzyl alcohol

: 5344-90-1
2-Aminobenzyl alcohol

Conditions

Conditions	Yield
With hydrogen; palladium In methanol at 25℃; under 2327.2 Torr; for 4.5h;	100%
With hydrogen; triethylamine In ethanol; water at 110℃; under 30003 Torr; for 24h; Autoclave;	99%
With sodium tetrahydroborate In water at 20℃; for 0.416667h; Green chemistry;	99%

: 612-25-9
2-Nitrobenzyl alcohol

: 552-89-6
2-nitro-benzaldehyde

Conditions

Conditions	Yield
With oxygen; perruthenate modified mesoporous silicate MCM-41 In toluene at 80℃; for 3h; Oxidation;	100%
With butyltriphenylphosphonium chlorochromate In acetonitrile for 2.5h; Heating;	100%
With 1H-imidazole; [bis(acetoxy)iodo]benzene In dichloromethane at 20℃; for 2h;	100%

: 75-44-5
phosgene

: 612-25-9
2-Nitrobenzyl alcohol

: 42854-99-9
o-nitrobenzyl chloroformate

Conditions

Conditions	Yield
In tetrahydrofuran; toluene at 20℃; for 18h;	100%
In tetrahydrofuran; toluene for 21h; Esterification;	99%
In 1,4-dioxane for 24h; Ambient temperature;

: 612-25-9
2-Nitrobenzyl alcohol

polymer, ring-opening metathesis polymerization, degree of polymerization 60; monomer(s): 2-chlorosulfonyl-5-norbornene; ethyl vinyl ether: polymer, ring-opening metathesis polymerization, degree of polymerization 60; monomer(s): 2-chlorosulfonyl-5-norbornene; ethyl vinyl ether

polymer, degree of polymerization 60; monomer(s): 2-chlorosulfonyl-5-norbornene; ethyl vinyl ether; 2-nitrobenzyl alcohol: polymer, degree of polymerization 60; monomer(s): 2-chlorosulfonyl-5-norbornene; ethyl vinyl ether; 2-nitrobenzyl alcohol

Conditions

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃;	100%

: 612-25-9
2-Nitrobenzyl alcohol

: 572-09-8
2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide

: 34546-55-9
2-nitrobenzyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside

Conditions

Conditions	Yield
With iodine; silver carbonate In dichloromethane at 20℃; for 16h; Molecular sieve; Inert atmosphere;	100%
With iodine; 2,3-dicyano-5,6-dichloro-p-benzoquinone In acetonitrile for 4h; Molecular sieve; Inert atmosphere;	91%

: 612-25-9
2-Nitrobenzyl alcohol

: 18162-48-6
tert-butyldimethylsilyl chloride

: 73961-59-8
tert-Butyl-dimethyl-(2-nitro-benzyloxy)-silane

Conditions

Conditions	Yield
With ferric hydrogen sulphate; triethylamine In acetonitrile at 20℃; for 30h; Inert atmosphere; chemoselective reaction;	100%

: 612-25-9
2-Nitrobenzyl alcohol

: 41882-63-7
(2-(hydroxyamino)phenyl)methanol

Conditions

Conditions	Yield
With hydrazine hydrate at 60℃; for 1.16667h; Green chemistry; chemoselective reaction;	99%
With ethanol; ammonium chloride; zinc
With ammonium chloride; water; zinc weiteres Reagens: Alkohol;
(electrochemical reduction);
With ammonium chloride; zinc In 2-methoxy-ethanol; water at 20℃; for 0.25h;

: 612-25-9
2-Nitrobenzyl alcohol

: 124-63-0
methanesulfonyl chloride

: 163915-96-6
(2-nitrophenyl)methyl methanesulfonate

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 20℃; for 2h;	99%
With triethylamine In 1,4-dioxane at 15 - 25℃; for 1.5h;
With triethylamine In tetrahydrofuran at 20℃;

: 612-25-9
2-Nitrobenzyl alcohol

: 62-53-3
aniline

: 67-63-0
isopropyl alcohol

: 3-isopropoxy-2-phenyl-2H-indazole

Conditions

Conditions	Yield
With sulfuric acid at 25℃; for 4h; Catalytic behavior; Time; Solvent; UV-irradiation;	99%

...Expand

: 96-41-3
Cyclopentanol

: 612-25-9
2-Nitrobenzyl alcohol

: 62-53-3
aniline

: 3-(cyclopentyloxy)-2-phenyl-2H-indazole

Conditions

Conditions	Yield
With sulfuric acid at 25℃; for 4h; UV-irradiation;	99%

...Expand

: 612-25-9
2-Nitrobenzyl alcohol

: 77-78-1
dimethyl sulfate

: 38177-30-9
1-(methoxymethyl)-2-nitrobenzene

Conditions

Conditions	Yield
With potassium hydroxide; N-benzyl-N,N,N-triethylammonium chloride In dichloromethane; water	98%
Stage #1: 2-Nitrobenzyl alcohol With sodium carbonate In ethyl acetate; acetonitrile at 20℃; for 0.166667h; Stage #2: dimethyl sulfate In ethyl acetate; acetonitrile at 20 - 60℃; Solvent; Temperature;	97.8%
phase transfer catalysis;

: 612-25-9
2-Nitrobenzyl alcohol

: 58479-61-1
tert-butylchlorodiphenylsilane

: tert-butyl-(2-nitrobenzyloxy)diphenylsilane

Conditions

Conditions	Yield
With 1H-imidazole In N,N-dimethyl-formamide at 20℃; for 2h;	98%

: 1436-34-6
1,2-Epoxyhexane

: 612-25-9
2-Nitrobenzyl alcohol

: (S)-1-(2-nitrobenzyloxy)-2-hexanol

Conditions

Conditions	Yield
With chiral oligo-(salen)Co(OTs) complexes; lutidinium p-toluene sulfonate In acetonitrile at 4℃; for 24h;	98%

: 612-25-9
2-Nitrobenzyl alcohol

: 108-24-7
acetic anhydride

: 77376-01-3
acetic acid 2-nitro-benzyl ester

Conditions

Conditions	Yield
K5 In acetonitrile at 20℃; for 0.333333h;	98%
With bismuth(lll) trifluoromethanesulfonate In acetonitrile at 20℃; for 0.0833333h;	97%
(NH4)8[CeW10O36]*20H2O for 1.5h; Heating;	97%

: 612-25-9
2-Nitrobenzyl alcohol

: 93-97-0
benzoic acid anhydride

: 110786-18-0
2-nitrobenzyl benzoate

Conditions

Conditions	Yield
With bismuth(lll) trifluoromethanesulfonate In acetonitrile for 0.5h; Heating;	98%

: 612-25-9
2-Nitrobenzyl alcohol

: 64-19-7
acetic acid

: 77376-01-3
acetic acid 2-nitro-benzyl ester

Conditions

Conditions	Yield
With K5 for 1.5h; Heating;	98%
With bismuth(lll) trifluoromethanesulfonate at 20℃; for 1h;	98%
With yttrium iron garnet In neat (no solvent) at 80℃; for 0.333333h; Green chemistry;	87%

: 612-25-9
2-Nitrobenzyl alcohol

: 29872-21-7
2-nitrobenzyl iodide

Conditions

Conditions	Yield
With 4-aminophenyl diphenylphosphinite; iodine In dichloromethane at 20℃; for 2h;	98%
With aluminum(III) hydrogen sulfate; potassium iodide In hexane for 2h; Heating;	90%
With toluene-4-sulfonic acid; potassium iodide for 0.0222222h; microwave irradiation;	82%

: 612-25-9
2-Nitrobenzyl alcohol

: 98-59-9
p-toluenesulfonyl chloride

: 20444-09-1
2-nitrobenzyl p-toluenesulfonate

Conditions

Conditions	Yield
With aluminum dodecatungstophosphate at 20℃; for 0.25h;	98%
With sodium carbonate In water at 20℃; for 3h;	89%
With triethylamine In dichloromethane for 2h;	79%
	51%

: 612-25-9
2-Nitrobenzyl alcohol

: 31230-17-8
3-amino-5-methylpyrazole

: 109-77-3
malononitrile

: 1313199-48-2
6-amino-3-methyl-4-(2-nitrophenyl)-1H-pyrazolo[3,4-b]pyridine-5-carbonitrile

Conditions

Conditions	Yield
With aluminum(III) hydrogen sulfate at 20℃; for 0.05h; Green chemistry;	98%

...Expand

: 606-23-5
1H-indene-1,3(2H)-dione

: 612-25-9
2-Nitrobenzyl alcohol

: 31230-17-8
3-amino-5-methylpyrazole

: 3-methyl-4-(2-nitrophenyl)indeno[1,2-b]pyrazolo-[4,3-e]pyridin-5(1H)-one

Conditions

Conditions	Yield
With aluminum(III) hydrogen sulfate at 20℃; for 0.0666667h; Green chemistry;	98%

...Expand

: 612-25-9
2-Nitrobenzyl alcohol

: 1-bromo-4-methoxy-10-methyl-6H-benzo[c]chromen-6-one

: 2-nitrobenzyl (R)-6'-bromo-2'-hydroxy-3'-methoxy-6-methyl-[1,1'-biphenyl]-2-carboxylate

Conditions

Conditions	Yield
With C29H28F6N4OS at 20℃; for 2h; enantioselective reaction;	98%

: 612-25-9
2-Nitrobenzyl alcohol

: 98-95-3
nitrobenzene

Conditions

Conditions	Yield
With 1,10-Phenanthroline; oxygen; copper diacetate; silver nitrate; sodium hydroxide In dimethyl sulfoxide at 140℃; under 3750.38 Torr; for 12h; Autoclave; Green chemistry;	98%

: 612-25-9
2-Nitrobenzyl alcohol

: 3958-60-9
2-nitrophenylmethyl bromide

Conditions

Conditions	Yield
With 4-aminophenyl diphenylphosphinite; bromine In dichloromethane at 20℃; for 0.416667h;	97%
With carbon tetrabromide; triphenylphosphine In tetrahydrofuran at 20℃; for 2h; Inert atmosphere;	94%
With phosphorus tribromide In dichloromethane at 0 - 20℃; for 1h; Inert atmosphere;	76%

: 612-25-9
2-Nitrobenzyl alcohol

: 95-54-5
1,2-diamino-benzene

: 2208-58-4
2-(2-nitrophenyl)-1H-benzimidazole

Conditions

Conditions	Yield
With air; Fe3O4 fabricated ZnO doped WO3 nanoparticle In ethanol at 20℃; for 2.5h; Irradiation; Green chemistry;	97%
With coomassie brilliant blue (CBB) coated on n-propylamine functionalized W-ZnO nanoparticles In ethanol at 25℃; for 2h; UV-irradiation; Green chemistry;	97%
With Ni0.5Co0.5Fe2O4 supported on arginine-grafted graphene oxide nanocomposite; air In acetonitrile at 80℃;	90%
Stage #1: 2-Nitrobenzyl alcohol With iodine; potassium carbonate In tert-butyl alcohol at 50℃; for 2h; Stage #2: 1,2-diamino-benzene In tert-butyl alcohol at 70℃; for 3h; Further stages.;	86%
With copper(II)-manganese(II) bimetallic complex immobilized on magnetite nanoparticles; air In neat (no solvent) at 70℃; for 4h; Green chemistry;	80%

2-NITROBENZYL ALCOHOL Specification

The 2-NITROBENZYL ALCOHOL , with the register number 612-25-9, is also known to us as rarechem al bd 0186;o-nitrobenzyl alcohol;o-nitrophenylcarbinol;labotest-bb lt01997457;(2-nitrophenyl)methanol;2-nitrobenzyl alcohol;2-nitro-benzenemethano;2-nitrobenzenemethanol .

The physical properties of this kind of chemcial are as following: (1)#H bond acceptors: 4 ; (2)#H bond donors: 1 ; (3)#Freely Rotating Bonds: 3 ; (4)Polar Surface Area: 55.05 ; (5)Index of Refraction: 1.597 ; (6)Molar Refractivity: 39.24 cm³ ; (7)Molar Volume: 115 cm³ ; (8)Polarizability: 15.55 ×10^-24 cm³ ; (9)Surface Tension: 57 dyne/cm ; (10)Density: 1.33 g/cm³ ; (11)Flash Point: 131.1 °C ; (12)Enthalpy of Vaporization: 53.68 kJ/mol ; (13)Boiling Point: 270 °C at 760 mmHg ; (14)Vapour Pressure: 0.00346 mmHg at 25°C .

It is a kind of white to light yellow crystal powder. As for its usage, it has various products categories: alcohols;c7 to c8;oxygen compounds. Being an irritant chemicals, it may cause inflammation to the skin or other mucous membranes. Besides, it is highly flammable and may catch fire in contact with air, only needing brief contact with an ignition source, for it has a very low flash point or evolve highly flammable gases in contact with water. What's more, it is corrosive as it may destroy living tissue on contact. Beside, its raw materials are including sodium carbonate, Bromine, 2-Nitrotoluene, and so on.

So while dealing with it, you should be very cautious. First, do not breathe dust; Secondly, avoid contacting with skin and eyes and if in case of accident or if you feel unwell seek medical advice immediately (show the label where possible). What's more, you should wear suitable protective clothing, gloves and eye/face protection; If in case of contact with eyes, rinse immediately with plenty of water and seek medical advice; And remember to keep away from sources of ignition - No smoking. If you need more safety information, you could refer to the WGK Germany 3.

In addition, you could refer to the following data information to get the molecular structure:
SMILES:[O-][N+](=O)c1ccccc1CO
InChI:InChI=1/C7H7NO3/c9-5-6-3-1-2-4-7(6)8(10)11/h1-4,9H,5H2
InChIKey:BWRBVBFLFQKBPT-UHFFFAOYAQ

Product Name

2-Nitrobenzyl alcohol

Synthetic route

2-NITROBENZYL ALCOHOL Specification

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