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7595-31-5

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7595-31-5 Usage

Chemical Properties

Yellow Solid

Check Digit Verification of cas no

The CAS Registry Mumber 7595-31-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,9 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7595-31:
(6*7)+(5*5)+(4*9)+(3*5)+(2*3)+(1*1)=125
125 % 10 = 5
So 7595-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O4/c1-13-7-3-5(9)6(10(11)12)4-8(7)14-2/h3-4H,9H2,1-2H3

7595-31-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-Dimethoxy-2-nitroaniline

1.2 Other means of identification

Product number -
Other names 2-nitro-4,5-dimethoxyaniline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7595-31-5 SDS

7595-31-5Synthetic route

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene
99069-17-7

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
With potassium hydroxide In methanol; water for 0.5h; Heating;95%
With hydrogenchloride
With hydrogenchloride
N-(4,5-dimethoxy-2-nitrophenyl)pyrimidin-2-amine

N-(4,5-dimethoxy-2-nitrophenyl)pyrimidin-2-amine

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Stage #1: N-(4,5-dimethoxy-2-nitrophenyl)pyrimidin-2-amine With triethylsilane; trifluoroacetic acid at 50℃; Inert atmosphere;
Stage #2: With acetic acid; hydrazine In methanol at 20℃; Inert atmosphere; regioselective reaction;
76%
4,5-dimethoxy-1,2-dinitrobenzene
3395-03-7

4,5-dimethoxy-1,2-dinitrobenzene

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
With benzophenone; triethylamine In isopropyl alcohol for 1h; Irradiation;19%
With ammonia at 150℃;
With ethanol; palladium Hydrogenation;
With hydrogenchloride; tin(ll) chloride
4,5-dimethoxy-1,2-dinitrobenzene
3395-03-7

4,5-dimethoxy-1,2-dinitrobenzene

dimethyl amine
124-40-3

dimethyl amine

A

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

B

4,5-dinitro-2-methoxyaniline
20278-59-5

4,5-dinitro-2-methoxyaniline

C

2,4-diamino-5-nitroanisole

2,4-diamino-5-nitroanisole

D

5,6-dimethoxy-2,1,3-benzoxadiazole
111611-40-6

5,6-dimethoxy-2,1,3-benzoxadiazole

E

5-dimethylamino-6-methoxybenzofurazane

5-dimethylamino-6-methoxybenzofurazane

F

N,N-dimethyl-4,5-dinitro-2-methoxyaniline

N,N-dimethyl-4,5-dinitro-2-methoxyaniline

Conditions
ConditionsYield
In methanol for 4h; Product distribution; Mechanism; Irradiation; different amines, reagents, solvent and reaction time;A 19%
B n/a
C n/a
D 13%
E n/a
F n/a
4,5-dimethoxy-1,2-dinitrobenzene
3395-03-7

4,5-dimethoxy-1,2-dinitrobenzene

ammonium acetate
631-61-8

ammonium acetate

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
at 130 - 135℃;
3,4-dimethoxy-2-nitroaniline
30710-17-9

3,4-dimethoxy-2-nitroaniline

A

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

B

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene
99069-17-7

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene

Conditions
ConditionsYield
With phosphoric acid; acetic acid at 140 - 160℃;
methanol
67-56-1

methanol

4,5-dimethoxy-1,2-dinitrobenzene
3395-03-7

4,5-dimethoxy-1,2-dinitrobenzene

ammonia
7664-41-7

ammonia

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
at 150℃;
at 125℃;
hydrogenchloride
7647-01-0

hydrogenchloride

4,5-dimethoxy-1,2-dinitrobenzene
3395-03-7

4,5-dimethoxy-1,2-dinitrobenzene

tin (II)-chloride

tin (II)-chloride

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

phosphoric acid
86119-84-8, 7664-38-2

phosphoric acid

3,4-dimethoxy-2-nitroaniline
30710-17-9

3,4-dimethoxy-2-nitroaniline

acetic acid
64-19-7

acetic acid

A

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

B

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene
99069-17-7

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene

Conditions
ConditionsYield
at 140 - 160℃;
acetoacetic acid-(4,5-dimethoxy-2-nitro-anilide)

acetoacetic acid-(4,5-dimethoxy-2-nitro-anilide)

mineral oil

mineral oil

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
at 230℃;
3,4-dimethoxynitrobenzene
709-09-1

3,4-dimethoxynitrobenzene

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
2: 95 percent / KOH / H2O; methanol / 0.5 h / Heating
View Scheme
Multi-step reaction with 2 steps
1: nitric acid
2: tin (II)-chloride; alcoholic hydrochloric acid
View Scheme
With potassium tert-butylate; N-methoxylamine hydrochloride; copper diacetate In N,N-dimethyl-formamide at -10 - 15℃;
1,2-dimethoxybenzene
91-16-7

1,2-dimethoxybenzene

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 90 percent / fuming nitric acid / acetic acid / 0.5 h / Ambient temperature
2: 19 percent / benzophenone, triethylamine / propan-2-ol / 1 h / Irradiation
View Scheme
Multi-step reaction with 2 steps
1: glacial acetic acid; aqueous nitric acid / <40 / anschliessendes Behandeln mit Salpetersaeure <30grad
2: methanol.ammonia / 150 °C
View Scheme
3',4'-dimethoxyacetanilide
881-70-9

3',4'-dimethoxyacetanilide

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: nitric acid
2: sulfuric acid / 100 °C
View Scheme
Multi-step reaction with 2 steps
1: glacial acetic acid; nitric acid
2: concentrated hydrochloric acid
View Scheme
2-acetamido-4,5-dimethoxybenzoic acid
145352-75-6

2-acetamido-4,5-dimethoxybenzoic acid

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: nitric acid
2: sulfuric acid / 100 °C
View Scheme
4',5'-dimethoxy-2'-nitroacetophenone
4101-32-0

4',5'-dimethoxy-2'-nitroacetophenone

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: iron; aq.-ethanolic acetic acid
3: nitric acid; acetic acid / <-10
4: aq.-ethanolic hydrochloric acid
View Scheme
acetic acid-(2-acetyl-4,5-dimethoxy-anilide)
148842-95-9

acetic acid-(2-acetyl-4,5-dimethoxy-anilide)

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: nitric acid; acetic acid / <-10
2: aq.-ethanolic hydrochloric acid
View Scheme
2-amino-4,5-dimethoxyacetophenone
4101-30-8

2-amino-4,5-dimethoxyacetophenone

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 3 steps
2: nitric acid; acetic acid / <-10
3: aq.-ethanolic hydrochloric acid
View Scheme
1-(3,4-dimethoxyphenyl)ethanone
1131-62-0

1-(3,4-dimethoxyphenyl)ethanone

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 5 steps
1: aqueous nitric acid; sulfuric acid / -3 °C
2: iron; aq.-ethanolic acetic acid
4: nitric acid; acetic acid / <-10
5: aq.-ethanolic hydrochloric acid
View Scheme
3,4-dimethoxyaniline
6315-89-5

3,4-dimethoxyaniline

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

methanolic ammonia

methanolic ammonia

4,5-dimethoxy-1,2-dinitrobenzene
3395-03-7

4,5-dimethoxy-1,2-dinitrobenzene

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
With ammonia In methanol
C12H13N3O2

C12H13N3O2

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1.1: palladium diacetate; silver(I) nitrite; dipotassium peroxodisulfate; acetic acid / 1,2-dichloro-ethane / 80 °C / Inert atmosphere
2.1: trifluoroacetic acid; triethylsilane / 50 °C / Inert atmosphere
2.2: 20 °C / Inert atmosphere
View Scheme
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

methyl iodide
74-88-4

methyl iodide

N-methyl-2-nitro-4,5-dimethoxyaniline
4496-11-1

N-methyl-2-nitro-4,5-dimethoxyaniline

Conditions
ConditionsYield
With sodium hydride In N,N-dimethyl-formamide 0-5 deg C, 10 min; 0-5 deg C, 1 h; RT, 1 h;96%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

COCl2

COCl2

4,5-Dimethoxy-2-nitrophenyl Isocyanate
113475-67-5

4,5-Dimethoxy-2-nitrophenyl Isocyanate

Conditions
ConditionsYield
In xylene90%
methanol
67-56-1

methanol

glyoxylic acid ethyl ester
924-44-7

glyoxylic acid ethyl ester

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

α-(4,5-dimethoxy-2-nitrophenylamino)-α-methoxyacetic acid ethyl ester
663932-54-5

α-(4,5-dimethoxy-2-nitrophenylamino)-α-methoxyacetic acid ethyl ester

Conditions
ConditionsYield
for 17h; Condensation; Heating;89%
at 65℃; for 17h;89%
In toluene at 20℃; Heating / reflux; Dean-Stark trap;88.1%
cis,trans-2,5-dimethoxytetrahydrofuran
696-59-3

cis,trans-2,5-dimethoxytetrahydrofuran

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

4,5-dimethoxy-2-pyrrolo-1-nitrobenzene
56721-98-3

4,5-dimethoxy-2-pyrrolo-1-nitrobenzene

Conditions
ConditionsYield
With acetic acid for 0.166667h; Heating;85%
2,2'-Pyridil
492-73-9

2,2'-Pyridil

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

6,7-dimethoxy-2,3-di(pyridin-2-yl)quinoxaline

6,7-dimethoxy-2,3-di(pyridin-2-yl)quinoxaline

Conditions
ConditionsYield
With indium; acetic acid In methanol at 50℃; for 1h; Inert atmosphere;80%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

9,10-phenanthrenequinone
84-11-7

9,10-phenanthrenequinone

11,12-dimethoxydibenzo[a,c]phenazine
100436-09-7

11,12-dimethoxydibenzo[a,c]phenazine

Conditions
ConditionsYield
With indium; acetic acid In methanol for 12h; Reflux; Inert atmosphere;72%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

dimethylglyoxal
431-03-8

dimethylglyoxal

6,7-dimethoxy-2,3-dimethylquinoxaline
32388-00-4

6,7-dimethoxy-2,3-dimethylquinoxaline

Conditions
ConditionsYield
With indium; indium(III) chloride In methanol for 2h; Reflux; Inert atmosphere;68%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

benzil
134-81-6

benzil

6,7-dimethoxy-2,3-diphenylquinoxaline
32388-01-5

6,7-dimethoxy-2,3-diphenylquinoxaline

Conditions
ConditionsYield
With indium; indium(III) chloride In methanol for 0.833333h; Reagent/catalyst; Reflux; Inert atmosphere;65%
2,2'-thenil
7333-07-5

2,2'-thenil

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

6,7-dimethoxy-2,3-di-2-thiophenylquinoxaline
861883-42-3

6,7-dimethoxy-2,3-di-2-thiophenylquinoxaline

Conditions
ConditionsYield
With indium; acetic acid In methanol for 0.333333h; Reflux; Inert atmosphere;53%
6-bromo-5-nitro-benzo[1,3]dioxole-4-carboxylic acid methyl ester
33842-23-8

6-bromo-5-nitro-benzo[1,3]dioxole-4-carboxylic acid methyl ester

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

N-(4',5'-Dimethoxy-2'-nitrophenyl)-6-amino-4-carbomethoxy-5-nitro-1,3-benzdioxol
93415-83-9

N-(4',5'-Dimethoxy-2'-nitrophenyl)-6-amino-4-carbomethoxy-5-nitro-1,3-benzdioxol

Conditions
ConditionsYield
With copper; potassium carbonate In nitrobenzene for 0.25h; Heating;32%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

crotonaldehyde
123-73-9

crotonaldehyde

4-methyl-5,6-dimethoxy-8-nitroquinoline
64992-96-7

4-methyl-5,6-dimethoxy-8-nitroquinoline

Conditions
ConditionsYield
With phosphoric acid; orthoarsenic acid at 100℃; for 0.5h;30%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

methyl vinyl ketone
78-94-4

methyl vinyl ketone

A

8-amino-5,6-dimethoxy-4-methylquinoline
64992-95-6

8-amino-5,6-dimethoxy-4-methylquinoline

B

4-methyl-5,6-dimethoxy-8-nitroquinoline
64992-96-7

4-methyl-5,6-dimethoxy-8-nitroquinoline

Conditions
ConditionsYield
A n/a
B 27%
3-penten-2-one
625-33-2

3-penten-2-one

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

5,6-dimethoxy-2,4-dimethyl-8-nitroquinoline
82082-03-9

5,6-dimethoxy-2,4-dimethyl-8-nitroquinoline

Conditions
ConditionsYield
With phosphoric acid; orthoarsenic acid at 100℃; for 0.5h;26%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

acrolein
107-02-8

acrolein

5,6-dimethoxy-8-nitroquinoline
5333-02-8

5,6-dimethoxy-8-nitroquinoline

Conditions
ConditionsYield
With phosphoric acid; orthoarsenic acid at 100℃; for 0.5h;22%
With phosphoric acid; orthoarsenic acid at 100℃;
With phosphoric acid; arsenic(III) trioxide at 100℃; for 3h;
1-chloro-3-pentanone
32830-97-0

1-chloro-3-pentanone

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

5,6-dimethoxy-4-ethyl-8-nitroquinoline
98509-92-3

5,6-dimethoxy-4-ethyl-8-nitroquinoline

Conditions
ConditionsYield
With phosphoric acid at 85 - 93℃; for 2.5h;18%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

trans-3-penten-2-one
3102-33-8

trans-3-penten-2-one

A

8-amino-5,6-dimethoxy-2,4-dimethylquinoline
64993-02-8

8-amino-5,6-dimethoxy-2,4-dimethylquinoline

B

5,6-dimethoxy-2,4-dimethyl-8-nitroquinoline
82082-03-9

5,6-dimethoxy-2,4-dimethyl-8-nitroquinoline

Conditions
ConditionsYield
A n/a
B 14%
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

3,4-dimethoxynitrobenzene
709-09-1

3,4-dimethoxynitrobenzene

Conditions
ConditionsYield
Verkochen.Diazotization;
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

4,5-dimethoxybenzene-1,2-diamine
27841-33-4

4,5-dimethoxybenzene-1,2-diamine

Conditions
ConditionsYield
With hydrogenchloride; tin(ll) chloride
With hydrogen; nickel In tetrahydrofuran at 60 - 70℃;
With palladium on activated charcoal; hydrogen
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

acetic anhydride
108-24-7

acetic anhydride

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene
99069-17-7

4-Acetylamino-1,2-dimethoxy-5-nitrobenzene

4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

ethyl acetoacetate
141-97-9

ethyl acetoacetate

acetoacetic acid-(4,5-dimethoxy-2-nitro-anilide)

acetoacetic acid-(4,5-dimethoxy-2-nitro-anilide)

Conditions
ConditionsYield
at 160℃;
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

glycerol
56-81-5

glycerol

5,6-dimethoxy-8-nitroquinoline
5333-02-8

5,6-dimethoxy-8-nitroquinoline

Conditions
ConditionsYield
With arsenic(V) oxide; sulfuric acid
With arsenic(V) oxide; phosphoric acid; sulfuric acid at 80℃;
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

diethyl malonate
105-53-3

diethyl malonate

(4,5-Dimethoxy-2-nitrophenyl)-azomalonsaeurediethylester
26002-74-4

(4,5-Dimethoxy-2-nitrophenyl)-azomalonsaeurediethylester

Conditions
ConditionsYield
(i) aq. NaNO2, aq. HCl, (ii) /BRN= 774687/, NaOAc; Multistep reaction;
With cis-nitrous acid; potassium carbonate 1) 0 deg C; Multistep reaction;
4-amino-5-nitroveratrol
7595-31-5

4-amino-5-nitroveratrol

methyl vinyl ketone
78-94-4

methyl vinyl ketone

4-methyl-5,6-dimethoxy-8-nitroquinoline
64992-96-7

4-methyl-5,6-dimethoxy-8-nitroquinoline

Conditions
ConditionsYield
With phosphoric acid; orthoarsenic acid at 100℃; for 2h; Yield given;

7595-31-5Relevant articles and documents

High Turnover Pd/C Catalyst for Nitro Group Reductions in Water. One-Pot Sequences and Syntheses of Pharmaceutical Intermediates

Gallou, Fabrice,Li, Xiaohan,Lipshutz, Bruce H.,Takale, Balaram S.,Thakore, Ruchita R.

supporting information, p. 8114 - 8118 (2021/10/25)

Commercially available Pd/C can be used as a catalyst for nitro group reductions with only 0.4 mol % Pd loading. The reaction can be performed using either silane as a transfer hydrogenating agent or simply a hydrogen balloon (μ1 atm pressure). With this technology, a series of nitro compounds was reduced to the desired amines in high chemical yields. Both the catalyst and surfactant were recycled several times without loss of reactivity.

UV-absorbers for ophthalmic lens materials

-

Page/Page column 7; 8, (2010/10/03)

UV absorbing compounds that are particularly useful in ophthalmic devices are disclosed.

Benzimidazolinone derivatives

-

, (2008/06/13)

Benzimidazolinone derivatives of the general formula (I): STR1 wherein R1, R2 and R3, which may be the same or different, each is a hydrogen or halogen atom or a lower alkyl, halo-lower alkyl, hydroxy-lower alkyl, hydroxyl, lower alkoxy, aryloxy, acyl, cyano, carboxyl, a lower alkoxycarbonyl, carbamoyl, nitro or nitrogen-containing 5- or 6-membered heterocyclic group; A is an ethylene group which may optionally have at least one branch; R4 and R5, which may be the same or different, each is a lower alkyl group or R4 and R5, together with the adjacent nitrogen atom, represent a pyrrolidinyl, piperidino or a morpholino group provided that when STR2 is a piperidino or diethylamino group, at least one of R1, R2 and R3 is other than a hydrogen atom, or pharmaceutically acceptable salts thereof, methods of producing the same and pharmaceutical compositions containing the same are disclosed. Pharmacologically, the above compounds (I) have pulmonary surfactant secretion promoting activity.

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