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Benzonitrile, 3-amino-4-nitro-

Product Name
Benzonitrile, 3-amino-4-nitro-
CAS No.
99512-10-4
Chemical Name
Benzonitrile, 3-amino-4-nitro-
Synonyms
3-amino-4-nitrobenzonitrile;Benzonitrile, 3-amino-4-nitro-
CBNumber
CB01865545
Molecular Formula
C7H5N3O2
Formula Weight
163.13
MOL File
99512-10-4.mol
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Benzonitrile, 3-amino-4-nitro- Property

storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
Appearance
Yellow to orange Solid
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Safety

RIDADR 
3439
HazardClass 
6.1
PackingGroup 
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

TRC
Product number
A615095
Product name
3-Amino-4-nitrobenzonitrile
Packaging
500mg
Price
$70
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA140196
Product name
3-Amino-4-nitrobenzonitrile
Packaging
1g
Price
$63
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA140196
Product name
3-Amino-4-nitrobenzonitrile
Packaging
2g
Price
$109
Updated
2021/12/16
AK Scientific
Product number
W9876
Product name
3-Amino-4-nitrobenzonitrile
Packaging
1g
Price
$117
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA140196
Product name
3-Amino-4-nitrobenzonitrile
Packaging
5G
Price
$217
Updated
2021/12/16
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Benzonitrile, 3-amino-4-nitro- Chemical Properties,Usage,Production

Synthesis

1635-61-6

99512-10-4

5-Chloro-2-nitroaniline (6.902 g, 40 mmol) was used as a raw material and mixed with Zn(CN)2 (2.818 g, 24 mmol) and Pd(PPh3)4 (2.311 g, 2 mmol) in DMF (40 mL). The reaction mixture was heated to 120 °C for 4 days. After completion of the reaction, it was cooled to room temperature. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was separated, washed with brine, dried (MgSO4), filtered, and concentrated under vacuum. The residue was purified by fast column chromatography on silica gel using 4:1 hexane/ethyl acetate as eluent to give 1.49 g (23% yield) of 3-amino-4-nitrobenzonitrile.

References

[1] Patent: WO2004/76424, 2004, A1. Location in patent: Page 268

Benzonitrile, 3-amino-4-nitro- Preparation Products And Raw materials

Raw materials

Preparation Products

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Benzonitrile, 3-amino-4-nitro- Suppliers

PharmaBlock Sciences (Nanjing),Inc.
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China
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021-58099652-8005 13585536065
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021-58099609
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Country
China
ProdList
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18729
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NovoChemy Ltd.
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