rotundine

  • CAS No.: 483-14-7
  • Purity: 99%
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Factory supply rotundine 483-14-7 with sufficient production capacity

  • Molecular Formula: C21H25NO4
  • Molecular Weight: 355.434
  • Appearance/Colour: Off-white solid 
  • Melting Point: 141-143 °C 
  • Boiling Point: 482.9 °C at 760 mmHg 
  • PKA: 6.53±0.20(Predicted) 
  • Flash Point: 138.7 °C 
  • PSA: 40.16000 
  • Density: 1.23 g/cm3 
  • LogP: 3.31440 

483-14-7 Relevant articles

Total Synthesis of (-)-Canadine, (-)-Rotundine, (-)-Sinactine, and (-)-Xylopinine Using a Last-Step Enantioselective Ir-Catalyzed Hydrogenation

Chen, Fener,Chen, Wenchang,Chen, Yu,Jiang, Meifen,Li, Weijian,Tang, Pei,Yang, Zhi

, p. 8143 - 8153 (2021/06/28)

A concise asymmetric total synthesis of ...

Method for synthesizing tetrahydroberberine and derivatives thereof

-

Paragraph 0094-0099, (2021/07/08)

The invention provides a method for synt...

Asymmetric total synthesis and identification of tetrahydroprotoberberine derivatives as new antipsychotic agents possessing a dopamine D1, D2 and serotonin 5-HT1A multi-action profile

Sun, Haifeng,Zhu, Liyuan,Yang, Huicui,Qian, Wangke,Guo, Lin,Zhou, Shengbin,Gao, Bo,Li, Zeng,Zhou, Yu,Jiang, Hualiang,Chen, Kaixian,Zhen, Xuechu,Liu, Hong

, p. 856 - 868 (2013/03/13)

An effective and rapid method for the mi...

Asymmetric synthesis of (S)-(-)-tetrahydropalmatine and (S)-(-)-canadine via a sulfinyl-directed Pictet-Spengler cyclization

Mastranzo, Virginia M.,Olivares Romero, José Luis,Yuste, Francisco,Ortiz, Benjamín,Sánchez-Obregón, Rubén,García Ruano, José L.

experimental part, p. 1266 - 1271 (2012/02/15)

(S)-(-)-Tetrahydropalmatine 2 and (S)-(-...

483-14-7 Process route

2,3,9,10-tetramethoxy-5,8-dihydro-6H-isoquinolino[3,2-α]isoquinoline
26067-60-7

2,3,9,10-tetramethoxy-5,8-dihydro-6H-isoquinolino[3,2-α]isoquinoline

tetrahydropalmatine
483-14-7,2934-97-6,3520-14-7,10097-84-4,84-38-8

tetrahydropalmatine

Conditions
Conditions Yield
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; (R,R)-1,1'-bis{(R)-4,5-dihydro-3H-dinaphtho[1,2-c:2',1'-e]-phosphepino}ferrocene; hydrogen; acetic acid; potassium bromide; In dichloromethane; at 25 ℃; for 72h; under 60804.1 Torr; enantioselective reaction; Inert atmosphere;
95%
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; hydrogen; 1,1'-bis{(S)-4,5-dihydro-3H-binaphtho[1,2-C:2',1'-e]phosphino}ferrocene; acetic acid; potassium bromide; In dichloromethane; at 20 ℃; for 100h; under 45603.1 Torr; Autoclave;
94%
formaldehyd
50-00-0,30525-89-4,61233-19-0

formaldehyd

(1S)-1-[3,4-dimethoxy-2-(S)-p-tolylsulfinyl]benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline
1356336-76-9

(1S)-1-[3,4-dimethoxy-2-(S)-p-tolylsulfinyl]benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

tetrahydropalmatine
483-14-7,2934-97-6,3520-14-7,10097-84-4,84-38-8

tetrahydropalmatine

Conditions
Conditions Yield
formaldehyd; (1S)-1-[3,4-dimethoxy-2-(S)-p-tolylsulfinyl]benzyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline; With trifluoroacetic acid; In toluene; at 140 ℃; for 0.5h; Microwave irradiation;
With sodium hydroxide; In water; pH=8;
56%

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