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  • Product Namep-Aminobenzamide
  • CasNo. 2835-68-9
  • MFC7H8N2O
  • MW136.153
  • Purity
  • Appearanceoff-white to beige crystalline powder
  • Packing
  • Contact usInquiry

Product Details

CasNo： 2835-68-9

MF： C7H8N2O

Appearance： off-white to beige crystalline powder

Chinese Manufacturer Supply Best Quality 2835-68-9 with Efficient Shipping

  • Molecular Formula:C7H8N2O
  • Molecular Weight:136.153
  • Appearance/Colour:off-white to beige crystalline powder 
  • Vapor Pressure:4.84E-05mmHg at 25°C 
  • Melting Point:181-183 °C(lit.) 
  • Refractive Index:1.632 
  • Boiling Point:349 °C at 760 mmHg 
  • PKA:16.83±0.50(Predicted) 
  • Flash Point:164.9 °C 
  • PSA：69.11000 
  • Density:1.233 g/cm3 
  • LogP:1.64920 

p-Aminobenzamide(Cas 2835-68-9) Usage

Synthesis Reference(s)

Synthetic Communications, 25, p. 4025, 1995 DOI: 10.1080/00397919508011478

InChI:InChI=1/C7H8N2O/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,8H2,(H2,9,10)

2835-68-9 Relevant articles

The reduction of aromatic nitro groups on solid supports using sodium hydrosulfite (Na2S2O4)

Scheuerman,Tumelty

, p. 6531 - 6535 (2000)

An improved method for reducing aromatic...

Heterogeneous catalyzed reduction of polymer-bound nitroarenes

Roedel, Martin,Thieme, Florian,Buchholz, Herwig,Koenig, Burkhard

, p. 1181 - 1187 (2002)

Deposition of palladium as a catalyst on...

RhNPs/SBA-NH2: A high-performance catalyst for aqueous phase reduction of nitroarenes to aminoarenes at room temperature

Ganji, Saidulu,Enumula, Siva Sankar,Marella, Ravi Kumar,Rao, Kamaraju Seetha Rama,Burri, David Raju

, p. 1813 - 1819 (2014)

A RhNPs/SBA-NH2 catalyst with 2) as supp...

Ammonium sulphate - Magnesium promoted selective reduction of aromatic nitro compounds

Prajapati,Borah,Sandhu,Ghosh

, p. 4025 - 4028 (1995)

Various nitroarenes and 2,1,3-benzooxadi...

Industrial Cunninghamia lanceolata carbon supported FeO(OH) nanoparticles-catalyzed hydrogenation of nitroarenes

Fu, Lihua,Li, Dingzhong,Lu, Hao,Qiu, Renhua,Sun, Tulai,Xing, Chen,Yang, Tianbao

, (2022/01/11)

The development of green and efficient m...

Nickel Boride Catalyzed Reductions of Nitro Compounds and Azides: Nanocellulose-Supported Catalysts in Tandem Reactions

Proietti, Giampiero,Prathap, Kaniraj Jeya,Ye, Xinchen,Olsson, Richard T.,Dinér, Peter

, p. 133 - 146 (2021/11/04)

Nickel boride catalyst prepared in situ ...

Method for preparing amine through catalytic reduction of nitro compound by cyclic (alkyl) (amino) carbene chromium complex

-

Paragraph 0015, (2021/04/17)

The cyclic (alkyl) (amino) carbene chrom...

Highly efficient hydrogenation reduction of aromatic nitro compounds using MOF derivative Co-N/C catalyst

Dai, Yuyu,Li, Xiaoqing,Wang, Likai,Xu, Xiangsheng

, p. 22908 - 22914 (2021/12/24)

The direct hydrogenation reduction of ar...

2835-68-9 Process route

carbon monoxide
201230-82-2

carbon monoxide

para-nitrophenyl bromide
586-78-7

para-nitrophenyl bromide

4-aminobenzamide
2835-68-9

4-aminobenzamide

4-nitrobenzamide
619-80-7

4-nitrobenzamide

Conditions
Conditions Yield
With ammonia; palladium diacetate; catacxium A; In 1,4-dioxane; at 130 ℃; for 20h; under 3000.3 Torr; Autoclave;
52 %Chromat.
40 %Chromat.
p-bromobenzamide
698-67-9

p-bromobenzamide

4-aminobenzamide
2835-68-9

4-aminobenzamide

Conditions
Conditions Yield
With copper(I) oxide; 1-D-O-Methyl-chiro-inositol; ammonia; sodium hydroxide; In water; at 100 ℃; for 12h;
95%
With C24H32N2*ClCu; ammonia; potassium carbonate; In 1-methyl-pyrrolidin-2-one; methanol; at 90 ℃; for 24h; under 5171.62 Torr; Inert atmosphere;
93%
With ammonium hydroxide; ethylenediaminetetraacetic acid; potassium carbonate; copper(II) oxide; In water; at 100 ℃; for 12h; Sealed tube;
59%

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