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Home Thiazoles 1771-18-2
1771-18-2,MFCD00037838
Catalog No.:AA00251B

1771-18-2 | 2-Methoxyphenothiazine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$7.00   $5.00
- +
100g
95%
in stock  
$98.00   $69.00
- +
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00251B
Chemical Name:
2-Methoxyphenothiazine
CAS Number:
1771-18-2
Molecular Formula:
C13H11NOS
Molecular Weight:
229.2975
MDL Number:
MFCD00037838
SMILES:
COc1ccc2c(c1)Nc1c(S2)cccc1
NSC Number:
72107
Properties
Properties
 
BP:
408.1 °C at 760 mmHg  
Form:
Solid  
MP:
185-188 °C  
Storage:
Light sensitive;Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
248  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
4.1  

Downstream Synthesis Route

[1]Patent:DE940829,1952,

[1]BulletindelaSocieteChimiquedeFrance,1957,p.938,943,944

[2]HelveticaChimicaActa,1959,vol.42,p.259,264,269

[3]ActaChemicaScandinavica(1947),1961,vol.15,p.2043-2046

[1]BulletindelaSocieteChimiquedeFrance,1959,p.1816

[1]Patent:US2892839,1956,

[1]Patent:US2785160,1952,

Literature

Title: Effect of food on the pharmacokinetics and pharmacodynamics of R1663, an oral factor Xa inhibitor, in healthy male volunteers.

Journal: International journal of clinical pharmacology and therapeutics 20120801

Title: Crossover dose escalation study to assess safety, pharmacokinetics, and pharmacodynamics of single doses of R1663, an oral factor Xa inhibitor, in healthy male volunteers.

Journal: Journal of clinical pharmacology 20120401

Title: 1-(10H-Phenothia-zin-2-yl)ethanone.

Journal: Acta crystallographica. Section E, Structure reports online 20110201

Title: Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.

Journal: Bioorganic & medicinal chemistry letters 20101101

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SDS
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