PONICIDIN

Base Information

Chemical Name:PONICIDIN
CAS No.:64363-86-6
Molecular Formula:C₁₄H₁₈N₂O₂
Molecular Weight:246.309
Hs Code.:

Synonyms:1H-Indole-3-ethanaminium,a-carboxy-N,N,N-trimethyl-, innersalt, (?à)-

Suppliers and Price of PONICIDIN

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 2 raw suppliers

Chemical Property of PONICIDIN

Chemical Property:

PSA：55.92000
LogP:0.53510

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of PONICIDIN

There total 9 articles about PONICIDIN which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 24.0%

: 54648-79-2
O-Methyl-N,N'-diisopropylisourea

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

: 64363-86-6,487-58-1,12673-47-1,97045-39-1
α-N,N,N-trimethyltryptophan betaine

Guidance literature:: In methanol; for 408h; Ambient temperature;
DOI:10.1016/S0040-4020(01)89759-3

Reference yield:

: 485-80-3,15519-60-5,60018-85-1,60018-86-2,79845-28-6
S-adenosyl-L-methionine

: 73-22-3,27732-43-0,80206-30-0,27813-82-7
L-Tryptophan

: 2812-40-0
N,N-α-dimethyl-L-tryptophan

: 64363-86-6,487-58-1,12673-47-1,97045-39-1
α-N,N,N-trimethyltryptophan betaine

: 526-31-8
L-abrine

Guidance literature:: With adenine deaminase; recombinant (SAM)-dependent tryptophan methyltransferase from Psilocybe serbica FSU₁₂₄₁₆; SAH-nucleosidase; In aq. buffer; at 25 ℃; for 4h; pH=8; Catalytic behavior; Enzymatic reaction;
DOI:10.1002/cbic.201800336