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Home > products > API Active Pharmaceutical Ingredient > Suvorexant CAS 1030377-33-3 API Active Pharmaceutical Ingredient

Suvorexant CAS 1030377-33-3 API Active Pharmaceutical Ingredient

Product Details

Place of Origin: China

Brand Name: Sunshine

Certification: ISO,COA

Model Number: 1030377-33-3

Payment & Shipping Terms

Minimum Order Quantity: Negotiation

Price: Negotiation

Packaging Details: Aluminum Foil Bag, Drum

Delivery Time: 7-15 days

Payment Terms: T/T, L/C, D/A, Western Union

Supply Ability: TON

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1030377-33-3 API Active Pharmaceutical Ingredient

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Suvorexant API Active Pharmaceutical Ingredient

CAS NO::
1030377-33-3
Appearance::
White To Pale Beige Solid
Molecular Formula::
C23H23ClN6O2
Molecular Weight::
450.92100
EINECS NO::
685-109-7
MDL NO::
NA
CAS NO::
1030377-33-3
Appearance::
White To Pale Beige Solid
Molecular Formula::
C23H23ClN6O2
Molecular Weight::
450.92100
EINECS NO::
685-109-7
MDL NO::
NA
Suvorexant CAS 1030377-33-3 API Active Pharmaceutical Ingredient

Product Description:

Product Name: suvorexant CAS NO: 1030377-33-3

 

 

Synonyms:

[(7R)-4-(5-Chloro-1,3-benzoxazol-2-yl)-7-methyl-1,4-diazepan-1-yl][5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone;

[(7R)-4-(5-chloro-1,3-benzoxazol-2-yl)-7-methyl-1,4-diazepan-1-yl]-[5-methyl-2-(triazol-2-yl)phenyl]methanone;

[(R)-4-(5-chlorobenzoxazol-2-yl)-7-methyl-[1,4]diazepan-1-yl]-(5-methyl-2-[1,2,3]triazol-2-yl-phenyl)methanone;

 

 

Chemical & Physical Properties:

Appearance: White to pale beige solid

Assay :≥98.0%+

Density: 1.419 g/cm3

Boiling Point: 669.803℃ at 760 mmHg

Flash Point: 358.884℃

Vapor Pressure: 0.0±2.0 mmHg at 25℃

 

 

Suvorexant, sold under the trade name Belsomra, is a medication for the treatment of insomnia. It is effective for insomnia, at least for four weeks and as compared to a placebo.

 

 

Suvorexant is a selective, dual orexin receptor antagonist made by Merck & Co. It was approved for sale by the U.S. Food and Drug Administration (FDA) on August 13, 2014. The U.S. Drug Enforcement Administration (DEA) has placed it on the list of schedule IV controlled substances, as it may lead to limited physical dependence or psychological dependence relative to the drugs or other substances in schedule III. The potential for psychological dependence is similar to that of zolpidem. The drug became available in Japan in November 2014 and in the United States in February 2015.

 

 

 

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Products under patent are offered for R & D purpose only. However, the final responsibility lies exclusively with the buyer.