N(4),N(4),O(2')-Trimethylcytidine

Base Information

Chemical Name:N(4),N(4),O(2')-Trimethylcytidine
CAS No.:34218-81-0
Molecular Formula:C₁₂H₁₉N₃O₅
Molecular Weight:285.3
Hs Code.:
DSSTox Substance ID:DTXSID60187801
Nikkaji Number:J2.140.785B
Wikidata:Q83059549
Mol file:34218-81-0.mol

Synonyms:N(4), N(4), O(2')-trimethylcytidine;NNO-TMC

Suppliers and Price of N(4),N(4),O(2')-Trimethylcytidine

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

Biosynth Carbosynth
N4,N4,2’-O-Trimethylcytidine
10 mg
$ 400.00

Biosynth Carbosynth
N4,N4,2’-O-Trimethylcytidine
5 mg
$ 300.00

Biosynth Carbosynth
N4,N4,2’-O-Trimethylcytidine
2 mg
$ 150.00

Biosynth Carbosynth
N4,N4,2’-O-Trimethylcytidine
1 mg
$ 100.00

Biosynth Carbosynth
N4,N4,2’-O-Trimethylcytidine
25 mg
$ 750.00

AK Scientific
N(4),N(4),O(2')-Trimethylcytidine
25mg
$ 1062.00

AK Scientific
N(4),N(4),O(2')-Trimethylcytidine
10mg
$ 590.00

AK Scientific
N(4),N(4),O(2')-Trimethylcytidine
5mg
$ 455.00

Total 10 raw suppliers

Chemical Property of N(4),N(4),O(2')-Trimethylcytidine

Chemical Property:

Boiling Point:470.7°Cat760mmHg
Flash Point:238.5°C
PSA：97.05000
Density:1.44g/cm³
LogP:-1.42510
XLogP3:-1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:285.13247072
Heavy Atom Count:20
Complexity:437

Purity/Quality:

97% ^*data from raw suppliers

N4,N4,2’-O-Trimethylcytidine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C1=NC(=O)N(C=C1)C2C(C(C(O2)CO)O)OC
Isomeric SMILES:CN(C)C1=NC(=O)N(C=C1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)OC

Technology Process of N(4),N(4),O(2')-Trimethylcytidine

There total 8 articles about N(4),N(4),O(2')-Trimethylcytidine 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: 96.0%

: 110567-20-9
4,4-N,N-dimethyl-3',5'-(1,1,3,3-tetraisopropyl-1,3-disilyl)-2'-O-methylcytidine

: 34218-81-0
N4,N4,2’-O-trimethylcytidine

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 108782-90-7
1-(3',5'-O-1,1,3,3-tetraisopropyl-1,3-disilyl)-β-D-ribofuranosyl-4-(2-nitrophenyl)-2-pyrimidinone

: 34218-81-0
N4,N4,2’-O-trimethylcytidine

Guidance literature:: Multi-step reaction with 3 steps

1: 81 percent / silver oxide / acetone / 72 h / 20 °C

2: 98 percent / triethylamine / ethanol / 20 °C

3: 96 percent / tetrabutylammonium fluoride / tetrahydrofuran / 20 °C

With tetrabutyl ammonium fluoride; triethylamine; silver(l) oxide; In tetrahydrofuran; ethanol; acetone;

Reference yield:

: 110567-19-6
1-(3',5'-O-1,1,3,3-tetraisopropyl-1,3-disilyl)-β-D-ribofuranosyl-2'-O-methyl-4-(2-nitrophenyl)-2-pyrimidinone

: 34218-81-0
N4,N4,2’-O-trimethylcytidine

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / triethylamine / ethanol / 20 °C

2: 96 percent / tetrabutylammonium fluoride / tetrahydrofuran / 20 °C

With tetrabutyl ammonium fluoride; triethylamine; In tetrahydrofuran; ethanol;