C₃₁H₂₄ClN₅O₃

Base Information

Chemical Name:C₃₁H₂₄ClN₅O₃
CAS No.:615538-51-7
Molecular Formula:C₃₁H₂₄ClN₅O₃
Molecular Weight:550.016
Hs Code.:

C<sub>31</sub>H<sub>24</sub>ClN<sub>5</sub>O<sub>3</sub>

Synonyms:

Suppliers and Price of C₃₁H₂₄ClN₅O₃

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

ChemScene
DC0-NH2 95.21%
10mg
$ 1500.00

ChemScene
DC0-NH2 95.21%
5mg
$ 980.00

ChemScene
DC0-NH2 95.21%
1mg
$ 550.00

Total 3 raw suppliers

Chemical Property of C₃₁H₂₄ClN₅O₃

Chemical Property:

Boiling Point:847.6±65.0 °C(Predicted)
Density:1.537±0.06 g/cm3(Predicted)

Purity/Quality:

97% ^*data from raw suppliers

DC0-NH2 95.21% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₁H₂₄ClN₅O₃

There total 9 articles about C₃₁H₂₄ClN₅O₃ 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: 90.0%

: 501441-05-0
1-(1S)-(chloromethyl)-5-hydroxy-3-{5-[(5-nitroindol-2-ylcarbonyl)amino]indole-2-carbonyl}-1,2-dihydro-3H-benz[e]indole

: 615538-51-7
C₃₁H₂₄ClN₅O₃

Guidance literature:: With hydrogenchloride; palladium 10% on activated carbon; hydrogen; In N,N-dimethyl acetamide;
DOI:10.1021/jm201284m

Reference yield:

: 16732-57-3
5-nitro-indole-2-carboxylic acid ethyl ester

: 615538-51-7
C₃₁H₂₄ClN₅O₃

Guidance literature:: Multi-step reaction with 5 steps

1.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 2068.65 Torr

2.1: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl acetamide / Inert atmosphere

3.1: sodium hydroxide / N,N-dimethyl acetamide; water / 1 h

3.2: pH 3

4.1: N,N-dimethyl acetamide; 1,2-dichloro-ethane / Inert atmosphere

5.1: hydrogenchloride; palladium 10% on activated carbon; hydrogen / N,N-dimethyl acetamide

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl acetamide; water; 1,2-dichloro-ethane;
DOI:10.1021/jm201284m

Reference yield:

: 501440-99-9
ethyl 5-((5-nitroindol-2-yl)carbonyl)aminoindole-2-carboxylate

: 615538-51-7
C₃₁H₂₄ClN₅O₃

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydroxide / N,N-dimethyl acetamide; water / 1 h

1.2: pH 3

2.1: N,N-dimethyl acetamide; 1,2-dichloro-ethane / Inert atmosphere

3.1: hydrogenchloride; palladium 10% on activated carbon; hydrogen / N,N-dimethyl acetamide

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; sodium hydroxide; In N,N-dimethyl acetamide; water; 1,2-dichloro-ethane;
DOI:10.1021/jm201284m