C₂₃H₂₃ClN₂O₃

Base Information

Chemical Name:C₂₃H₂₃ClN₂O₃
CAS No.:1208870-68-1
Molecular Formula:C₂₃H₂₃ClN₂O₃
Molecular Weight:410.9
Hs Code.:

C<sub>23</sub>H<sub>23</sub>ClN<sub>2</sub>O<sub>3</sub>

Synonyms:

Suppliers and Price of C₂₃H₂₃ClN₂O₃

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 0 raw suppliers

Chemical Property of C₂₃H₂₃ClN₂O₃

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₂₃H₂₃ClN₂O₃

There total 5 articles about C₂₃H₂₃ClN₂O₃ 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:

: 1208318-10-8
3-methyl-4-(1H-pyrrol-1-yl)benzamide

: 1208870-68-1
C₂₃H₂₃ClN₂O₃

Guidance literature:: Multi-step reaction with 6 steps

1: trichlorophosphate

2: toluene / Reflux

3: palladium 10% on activated carbon; hydrogen / ethanol

4: N-Bromosuccinimide

5: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate

6: dihydrogen peroxide; potassium carbonate / dimethyl sulfoxide / 20 °C

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; dihydrogen peroxide; sodium carbonate; potassium carbonate; trichlorophosphate; In ethanol; dimethyl sulfoxide; toluene; 1: Vilsmeier formylation / 2: Wittig reaction / 5: Suzuki coupling;
DOI:10.1021/ml200045s

Reference yield:

: 1208318-11-9
4-(2-formyl-1H-pyrrol-1-yl)-3-methylbenzonitrile

: 1208870-68-1
C₂₃H₂₃ClN₂O₃

Guidance literature:: Multi-step reaction with 5 steps

1: toluene / Reflux

2: palladium 10% on activated carbon; hydrogen / ethanol

3: N-Bromosuccinimide

4: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate

5: dihydrogen peroxide; potassium carbonate / dimethyl sulfoxide / 20 °C

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; dihydrogen peroxide; sodium carbonate; potassium carbonate; In ethanol; dimethyl sulfoxide; toluene; 1: Wittig reaction / 4: Suzuki coupling;
DOI:10.1021/ml200045s

Reference yield:

: 106037-36-9
4-amino-3-methylbenzamide

: 1208870-68-1
C₂₃H₂₃ClN₂O₃

Guidance literature:: Multi-step reaction with 7 steps

1: acetic acid

2: trichlorophosphate

3: toluene / Reflux

4: palladium 10% on activated carbon; hydrogen / ethanol

5: N-Bromosuccinimide

6: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate

7: dihydrogen peroxide; potassium carbonate / dimethyl sulfoxide / 20 °C

With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; dihydrogen peroxide; sodium carbonate; potassium carbonate; acetic acid; trichlorophosphate; In ethanol; dimethyl sulfoxide; toluene; 2: Vilsmeier formylation / 3: Wittig reaction / 6: Suzuki coupling;
DOI:10.1021/ml200045s