16800-67-2

  • Product Name:1,3-DIACETOXYINDOLE
  • Molecular Formula:C12H11NO3
  • Purity:99%
  • Molecular Weight:217.224
InquiryAdd to cart

Product Details;

CasNo: 16800-67-2

Molecular Formula: C12H11NO3

Appearance: Light brown solid

factory and supplier 16800-67-2 1,3-DIACETOXYINDOLE in stock

  • Molecular Formula:C12H11NO3
  • Molecular Weight:217.224
  • Appearance/Colour:Light brown solid 
  • Vapor Pressure:6.21E-05mmHg at 25°C 
  • Melting Point:80 °C 
  • Refractive Index:1.578 
  • Boiling Point:345.3 °C at 760 mmHg 
  • Flash Point:162.6 °C 
  • PSA:48.30000 
  • Density:1.21 g/cm3 
  • LogP:2.22670 

1,3-DIACETOXYINDOLE(Cas 16800-67-2) Usage

InChI:InChI=1/C12H11NO3/c1-8(14)13-7-12(16-9(2)15)10-5-3-4-6-11(10)13/h3-7H,1-2H3

16800-67-2 Relevant articles

Orally Effective Aminoalkyl 10H-Indolo[3,2-b]quinoline-11-carboxamide Kills the Malaria Parasite by Inhibiting Host Hemoglobin Uptake

Mudududdla, Ramesh,Mohanakrishnan, Dinesh,Bharate, Sonali S.,Vishwakarma, Ram A.,Sahal, Dinkar,Bharate, Sandip B.

, p. 2581 - 2598 (2018)

A series of indolo[3,2-b]quinoline-C11-c...

Pharmacological evaluation of novel PKR inhibitor indirubin-3-hydrazone in-vitro in cardiac myocytes and in-vivo in wistar rats

Udumula, Mary Priyanka,Bhat, Audesh,Mangali, Sureshbabu,Kalra, Jaspreet,Dhar, Indu,Sriram, Dharamrajan,Dhar, Arti

, p. 85 - 96 (2018)

Aims: Double stranded protein kinase R c...

A concise synthesis of the DNA-intercalating and antimalarial alkaloid cryptolepine and its fluorescence behaviour in solvents of different polarities

Lai, Tapan Kumar,Chatterjee, Asima,Banerji, Julie,Sarkar, Deboleena,Chattopadhyay, Nitin

, p. 1975 - 1983 (2008)

A microwave-induced rapid and facile syn...

Synthesis and biological evaluation of indoloquinoline alkaloid cryptolepine and its bromo-derivative as dual cholinesterase inhibitors

Nuthakki, Vijay K.,Mudududdla, Ramesh,Sharma, Ankita,Kumar, Ajay,Bharate, Sandip B.

, (2019)

Alkaloids have always been a great sourc...

-

Tighineanu,E. et al.

, p. 1887 - 1890 (1978)

-

Phenylimino Indolinone: A Green-Light-Responsive T-Type Photoswitch Exhibiting Negative Photochromism

Buma, Wybren Jan,Crespi, Stefano,Di Donato, Mariangela,Doria, Sandra,Feringa, Ben L.,Hilbers, Michiel F.,Kiss, Ferdinand L.,Simeth, Nadja A.,Stindt, Charlotte N.,Szymański, Wiktor,Toyoda, Ryojun,Wesseling, Sammo

supporting information, p. 25290 - 25295 (2021/10/25)

Imines are photoaddressable motifs usefu...

Construction of Oxepino[3,2-b]indoles via [4+3] Annulation of 2-Ylideneoxindoles with Crotonate-Derived Sulfur Ylides

Fei, Xing-Hai,Guan, Xiang,He, Bin,Li, Zong-Qin,Wang, Da-Peng,Yang, Fen-Fen,Yang, Yuan-Yong,Zhao, Yong-Long,Zhou, Meng

supporting information, p. 3018 - 3024 (2021/06/26)

A [4+3] annulation of 2-ylideneoxindoles...

Indirubin Derivatives as Dual Inhibitors Targeting Cyclin-Dependent Kinase and Histone Deacetylase for Treating Cancer

An, Jianxiong,Cao, Zhuoxian,Gu, Zhicheng,He, Bin,Li, Yan,Li, Yongjun,Lin, Hening,Lin, Shuxian,Liu, Ting,Wang, Jie,Wang, Pan,Yang, Fenfen,Zhao, Yonglong

, p. 15280 - 15296 (2021/10/25)

To utilize the unique scaffold of a natu...

16800-67-2 Process route

2-(N-(carboxymethyl)acetamido)benzoic acid
16851-69-7

2-(N-(carboxymethyl)acetamido)benzoic acid

acetic anhydride
108-24-7

acetic anhydride

N,O-diacetylindoxyl
16800-67-2

N,O-diacetylindoxyl

Conditions
Conditions Yield
With pyridine; at 55 - 60 ℃; for 24h;
90%
With triethylamine; for 0.5h; Inert atmosphere; Schlenk technique; Reflux;
89%
With triethylamine; In water; at 20 ℃; for 0.333333h; Heating / reflux;
86%
With triethylamine; for 0.0666667h; Microwave irradiation; Inert atmosphere;
86%
With triethylamine; at 100 ℃;
80%
With triethylamine; at 100 ℃;
80%
With triethylamine; Heating;
3-indoxyl acetate
608-08-2

3-indoxyl acetate

acetic anhydride
108-24-7

acetic anhydride

N,O-diacetylindoxyl
16800-67-2

N,O-diacetylindoxyl

Conditions
Conditions Yield
With dmap; In tetrahydrofuran; at 85 ℃; for 16h; Inert atmosphere; Schlenk technique; Sealed tube;
93%
With triethylamine; at 80 - 90 ℃; for 0.5h;
82%
With dmap; triethylamine; In tetrahydrofuran; for 3h; Heating / reflux;
67%

16800-67-2 Upstream products

  • 16800-68-3
    16800-68-3

    1-acetyl-2,3-dihydro-1H-indol-3-one

  • 108-24-7
    108-24-7

    acetic anhydride

  • 480-93-3
    480-93-3

    indoxyl

  • 612-42-0
    612-42-0

    phenylglycine-o-carboxylic acid

16800-67-2 Downstream products

  • 16078-30-1
    16078-30-1

    1-Acetyl-2,3-dihydro-1H-indole

  • 99293-86-4
    99293-86-4

    N-acetylindolin-3-ol

  • 33025-60-4
    33025-60-4

    1-(3-hydroxy-1H-indol-1-yl)ethanone

  • 110912-08-8
    110912-08-8

    1,1'-(3-oxoindoline-1,2-diyl)bis(ethan-1-one)

Relevant Products

Shopping Cart

Clear Inquiry