1968-05-4
- Product Name：3,3'-Diindolylmethane
- Molecular Formula：C17H14N2
- Purity：99%
- Molecular Weight：246.312
Product Details
Melting Point:167 °C
Purity:99%
Quality Factory Supply 99% Pure 3,3'-Diindolylmethane 1968-05-4 with Efficient Delivery
- Molecular Formula:C17H14N2
- Molecular Weight:246.312
- Melting Point:167 °C
- Boiling Point:504.8 °C at 760 mmHg
- PKA:16.91±0.30(Predicted)
- Flash Point:232.5 °C
- PSA：31.58000
- Density:1.271 g/cm3
- LogP:4.24000
1968-05-4 Relevant articles
Cooperative Cation-Binding Catalysis as an Efficient Approach for Enantioselective Friedel–Crafts Reaction of Indoles and Pyrrole
Kim, Mun Jong,Xue, Lu,Liu, Yidong,Paladhi, Sushovan,Park, Si Joon,Yan, Hailong,Song, Choong Eui
, p. 811 - 823 (2017)
In this study, we demonstrated the coope...
The cruciferous phytoalexins rapalexin A, brussalexin A and erucalexin: Chemistry and metabolism in Leptosphaeria maculans
Pedras, M. Soledade C.,Sarma-Mamillapalle, Vijay K.
, p. 3991 - 3996 (2012)
The interactions of the cruciferous phyt...
Synthesis and antibacterial evaluation of 3,3′-diindolylmethane derivatives
Roy, Sutapa,Gajbhiye, Rahul,Mandal, Madhumita,Pal, Churala,Meyyapan, Arumugam,Mukherjee, Joydeep,Jaisankar, Parasuraman
, p. 1371 - 1377 (2014)
Various 3,3′-diindolylmethane (DIM) deri...
Direct use of methanol as an alternative to formaldehyde for the synthesis of 3, 3′-bisindolylmethanes (3, 3′-BIMs)
Sun, Chunlou,Zou, Xiaoyuan,Li, Feng
, p. 14030 - 14033 (2013)
The article examines the direct use of m...
-
Beteiller,Colilla
, p. 3393,3402 (1972)
-
InCl3-HMTA as a methylene donor: One-pot synthesis of diindolylmethane (DIM) and its derivatives
Pradhan, Prasun K.,Dey, Sumit,Giri, Venkatachalam Sesha,Jaisankar, Parasuraman
, p. 1779 - 1782 (2005)
Treatment of indoles la-k with hexamethy...
N-Allylation And N-Benzylation Of 2-Phenylindole And Its Condensation With Carbonyl Compounds
Obynochnyi, A. A.,Anisimov, B. N.,Sergeeva, N. D.,Prostakov, N. S.
, p. 553 - 555 (1993)
By allylation and benzylation of 2-pheny...
Eco-friendly synthesis and study of new plant growth promoters: 3,3′-Diindolylmethane and its derivatives
Pal, Churala,Dey, Sumit,Mahato, Sanjit Kumar,Vinayagam, Jayaraman,Pradhan, Prasun K.,Giri, Venkatachalam Sesha,Jaisankar, Parasuraman,Hossain, Tanvir,Baruri, Shikhi,Ray, Debjit,Biswas, Suparna Mandal
, p. 4924 - 4928 (2007)
3,3′-Diindolylmethane (DIM) derivatives ...
A Novel Electrochemical Oxidation Reactions Utilizing Cyclodextrins. Anodic Oxidation of Indole-Cyclodextrin-Alcohol System
Suda, Kohji,Takanami, Toshikatsu
, p. 1915 - 1916 (1994)
The anodic oxidation of indoles (1) and ...
-
Leete,Marion
, p. 775,777 (1953)
-
Decarboxylative Coupling Reaction of 2-(1H-Indol-3-yl)acetic Acids with Indole, Azaindole, Benzimidazole and Indazole Derivatives
Pillaiyar, Thanigaimalai,Uzair, Muhammad,Ullah, Saif,Schnakenburg, Gregor,Müller, Christa E.
, p. 4286 - 4293 (2019)
3,3′-Diindolylmethanes (DIMs) are an imp...
-
Coker et al.
, p. 589 (1963)
-
Convenient synthesis of 5,6,11,12,17,18-hexahydrocyclononal[1,2-b:4,5-b′:7,8-b″] triindole, a Novel phytoestrogen
Staub, Richard E.,Bjeldanes, Leonard F.
, p. 167 - 169 (2003)
An efficient one-pot synthesis is descri...
Carbon transfer reactions with heterocycles-IV. Synthetic equivalence of perhydrooxazines with carbonyl compounds. A facile synthesis of streptindole and analogues
Singh,Singh
, p. 5897 - 5904 (1988)
-
Palladium catalyzed alkylation of indole via aliphatic C-H bond activation of tertiary amine
Ramachandiran,Muralidharan,Perumal
, p. 3579 - 3583 (2011)
Alkylation of indoles has been achieved ...
Well-Defined NNS-Mn Complex Catalyzed Selective Synthesis of C-3 Alkylated Indoles and Bisindolylmethanes Using Alcohols
Dutta, Bishal,Mondal, Avijit,Pal, Debjyoti,Sharma, Rahul,Srimani, Dipankar
, p. 3989 - 4000 (2022/03/27)
Herein, we demonstrated Mn-catalyzed sel...
Minor bioactive indoles from kimchi mirror the regioselectivity in indole-3-carbinol oligomerization
Cheng Qian, Jia,Jing Zhu, Wen,Liu, Dan,Ping Lin, Li,Xiang Tan, Ren
, (2022/03/07)
Kimchi is a globally consumed food with ...
Synthesis of bisindolylmethane, bispyrrolylmethane, and indolylpyrrolylmethane derivatives via reductive heteroarylation
Zhou, Hang,Huang, Zhuo,Huang, He,Song, Chuanjun,Chang, Junbiao
, (2021/07/25)
An efficient and general reductive heter...
Nickel-catalyzed C3-alkylation of indoles with alcohols: Via a borrowing hydrogen strategy
Hu, Miao,Jiang, Yong,Sun, Nan,Hu, Baoxiang,Shen, Zhenlu,Hu, Xinquan,Jin, Liqun
, p. 10057 - 10062 (2021/06/15)
An efficient method for the Ni-catalyzed...
1968-05-4 Process route
-
-
glucobrassicin
-
indole-3-carbinol
-
700-06-1
indole-3-carbinol
-
-
771-51-7
indole-3-acetonitrile
-
-
1968-05-4
3,3'-diindolylmethane
| Conditions | Yield |
|---|---|
|
With
myrosinase;
In
water;
at 37 ℃;
for 4h;
Mechanism;
|
|
|
With
myrosinase;
In
water;
for 40h;
Mechanism;
low water system;
|
-
-
glucobrassicin
-
indole-3-carbinol
-
700-06-1
indole-3-carbinol
-
-
771-51-7
indole-3-acetonitrile
-
-
1968-05-4
3,3'-diindolylmethane
| Conditions | Yield |
|---|---|
|
With
myrosinase;
In
water;
at 37 ℃;
for 4h;
Product distribution;
other solvent, other substrates;
|
1968-05-4 Upstream products
-
120-72-9
indole
-
50-00-0
formaldehyd
-
87-52-5
3-(Dimethylaminomethyl)indole
-
72687-70-8
N-((1H-indol-3-yl)methyl)-N-methylbenzenamine
1968-05-4 Downstream products
-
526-32-9
3-
-
53330-79-3
3-(4-nitro-phenylazo)-indole
-
61844-14-2
3-(p-nitrophenylazo)-2,3'-methylenedi-indole
-
666752-28-9
3,3'-methylenebis(1H-indole-1-carboxylic acid) 1,1'-bis(1,1-dimethylethyl) ester
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