C₅₁H₇₅N₁₂O₁₈P

Base Information

Chemical Name:C₅₁H₇₅N₁₂O₁₈P
CAS No.:508234-89-7
Molecular Formula:C₅₁H₇₅N₁₂O₁₈P
Molecular Weight:1175.2
Hs Code.:

C<sub>51</sub>H<sub>75</sub>N<sub>12</sub>O<sub>18</sub>P

Synonyms:C₅₁H₇₅N₁₂O₁₈P

Suppliers and Price of C₅₁H₇₅N₁₂O₁₈P

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 1 raw suppliers

Chemical Property of C₅₁H₇₅N₁₂O₁₈P

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₅₁H₇₅N₁₂O₁₈P

There total 14 articles about C₅₁H₇₅N₁₂O₁₈P 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:

: 187745-72-8
Di(tert-butyl)-N-(2-cyanoethyl)-N,N'-(ethan-1,2-diyl)bis

: 508234-89-7
C₅₁H₇₅N₁₂O₁₈P

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / H₂; KOH / Raney Ni / ethanol / 5 h / 2250.18 Torr

2: 80 percent / dicyclohexylcarbodiimide / CH₂Cl₂ / 3 h / 20 °C

3: 96 percent / aq. NaOH / tetrahydrofuran / 1 h

4: dicyclohexylcarbodiimide / CH₂Cl₂ / 0.5 h / 20 °C

5: 52 mg / aq. NaHCO₃; aq. NaOH / acetonitrile / 1 h / pH 8

With potassium hydroxide; sodium hydroxide; hydrogen; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; nickel; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile;
DOI:10.1016/S0968-0896(02)00311-5

Reference yield:

: 1019333-23-3
[2-(2-cyano-ethylamino)-ethyl]-carbamic acid tert-butyl ester

: 508234-89-7
C₅₁H₇₅N₁₂O₁₈P

Guidance literature:: Multi-step reaction with 6 steps

1: 12.90 g / CH₂Cl₂ / 12 h / 20 °C

2: 100 percent / H₂; KOH / Raney Ni / ethanol / 5 h / 2250.18 Torr

3: 80 percent / dicyclohexylcarbodiimide / CH₂Cl₂ / 3 h / 20 °C

4: 96 percent / aq. NaOH / tetrahydrofuran / 1 h

5: dicyclohexylcarbodiimide / CH₂Cl₂ / 0.5 h / 20 °C

6: 52 mg / aq. NaHCO₃; aq. NaOH / acetonitrile / 1 h / pH 8

With potassium hydroxide; sodium hydroxide; hydrogen; sodium hydrogencarbonate; dicyclohexyl-carbodiimide; nickel; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile;
DOI:10.1016/S0968-0896(02)00311-5

Reference yield:

: 64350-24-9
N²-isobutyryl-2'-deoxyguanosine

: 508234-89-7
C₅₁H₇₅N₁₂O₁₈P

Guidance literature:: Multi-step reaction with 5 steps

1: 87 percent / TsOH*H₂O / dimethylformamide / 10 h

2: tetrazole / acetonitrile / 0.42 h / 0 - 20 °C

3: 100 mg / I₂; pyridine / acetonitrile; tetrahydrofuran; H₂O / 0.42 h / 0 - 20 °C

4: TFA / CH₂Cl₂ / 0.5 h

5: 52 mg / aq. NaHCO₃; aq. NaOH / acetonitrile / 1 h / pH 8

With pyridine; 1H-tetrazole; sodium hydroxide; iodine; sodium hydrogencarbonate; toluene-4-sulfonic acid; trifluoroacetic acid; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0968-0896(02)00311-5