Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 118864-75-8
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Aluminum Foil Bag, Drum
Delivery Time: 7-15DAY
Payment Terms: L/C,D/P,T/T,D/A,Western Union,MoneyGram
Supply Ability: G,KG,TON
Appearance:: |
White Solid |
CAS NO:: |
118864-75-8 |
Molecular Formula:: |
C15H15N |
Molecular Weight:: |
209.28600 |
EINECS NO:: |
601-570-9 |
MDL NO:: |
MFCD08692036 |
Appearance:: |
White Solid |
CAS NO:: |
118864-75-8 |
Molecular Formula:: |
C15H15N |
Molecular Weight:: |
209.28600 |
EINECS NO:: |
601-570-9 |
MDL NO:: |
MFCD08692036 |
Product Description:
Product Name: (1S)-1-Phenyl-1,2,3,4-tetrahydroisoquinoline CAS NO: 118864-75-8
Synonyms:
(1S)-1-Phenyl-1,2,3,4-tetrahydro-isopquinoline;
Solifenacin Related Compound 11;
Solifenacin Succinate interMediate F;
Chemical & Physical Properties:
Appearance: White solid
Assay :≥99.00%
Density: 1.065
Boiling Point: 338℃
Melting Point: 80-82℃
Flash Point: 167℃
Refractive Index: 1.589
Vapor Pressure: 9.87E-05mmHg at 25℃
Safety Information:
HS Code: 2942000000
(S) -1-phenyl-1,2,3, 4-tetrahydroisoquinoline can be used to prepare sofinacin. Solifenacin succinate, CAS No. 242478-38-2, chemical name 1-azabicyclic [2.2.2] octan-8-yl -(1S) -1-phenyl-3, 4-dihydro-1H-isoquinoline-2-formate succinate, It is a selective muscarinic M3 receptor antagonist developed by Japan's Astellas Company. It was first marketed in the Netherlands, Germany, the United Kingdom and Denmark in 2004 and in China in 2009. So far, it has been marketed in more than 50 countries and regions around the world, and has become an important drug for the treatment of bladder overactivity (OAB) in Europe, the United States and Japan. Recommended by multiple authorities and guidelines. Its preparation is as follows: (S) -1-phenyl-3, 4-dihydro-1H-isoquinoline-2-formyl chloride (II) was obtained by condensation of (S) -1-phenyl-1,2,3, 4-tetrahydroisoquinoline (I) with triphosgene under the condition of organic base (weak base). Compound II was heated directly under the catalysis of organic base by one-pot method without separation. Solinacine succinate (IV) was prepared by condensation reaction with (R) -3-quinine cycloalcohol to obtain solinacine (III).
If you are interested in our products or have any questions, please feel free to contact us!
Products under patent are offered for R & D purpose only. However, the final responsibility lies exclusively with the buyer.