(9S)-Cinchonan-9-ol sulfate (2:1)

Modify Date: 2024-01-18 02:50:38

(9S)-Cinchonan-9-ol sulfate (2:1) Structure
(9S)-Cinchonan-9-ol sulfate (2:1) structure
Common Name (9S)-Cinchonan-9-ol sulfate (2:1)
CAS Number 5949-16-6 Molecular Weight 686.860
Density 1.61g/cm3 Boiling Point 169 °C(lit.)
Molecular Formula C38H46N4O6S Melting Point 38-40 °C(lit.)
MSDS USA Flash Point 148 °F

 Names

Name Cinchonine Sulfate Dihydrate
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.61g/cm3
Boiling Point 169 °C(lit.)
Melting Point 38-40 °C(lit.)
Molecular Formula C38H46N4O6S
Molecular Weight 686.860
Flash Point 148 °F
Exact Mass 686.313782
PSA 155.70000
LogP 6.63300
Index of Refraction 1.717

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
GD3800000
CAS REGISTRY NUMBER :
5949-16-6
LAST UPDATED :
198708
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C19-H22-N2-O.1/2H2-O4-S
MOLECULAR WEIGHT :
343.43

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
800 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 78,159,1943

 Safety Information

Hazard Codes Xi
Risk Phrases R36/37/38
Safety Phrases 26-36
RIDADR 1544
WGK Germany 3
RTECS GD3800000
Packaging Group III
Hazard Class 6.1(b)

 Articles24

More Articles
Mutation in the Plasmodium falciparum CRT protein determines the stereospecific activity of antimalarial cinchona alkaloids.

Antimicrob. Agents Chemother. 56(10) , 5356-64, (2012)

The Cinchona alkaloids are quinoline aminoalcohols that occur as diastereomer pairs, typified by (-)-quinine and (+)-quinidine. The potency of (+)-isomers is greater than the (-)-isomers in vitro and ...

A theoretical investigation on the Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetraisopropyl titanate.

Chemistry 19(5) , 1637-46, (2013)

The mechanism and the origin of selectivity of the asymmetric Strecker reaction catalyzed by a Ti(IV)-complex catalyst generated from a cinchona alkaloid, achiral substituted 2,2'-biphenol, and tetrai...

Organocatalytic asymmetric conjugate addition of 3-monosubstituted oxindoles to (E)-1,4-diaryl-2-buten-1,4-diones: a strategy for the indirect enantioselective furanylation and pyrrolylation of 3-alkyloxindoles.

Chemistry 18(21) , 6679-87, (2012)

An asymmetric conjugate addition of 3-monosubstituted oxindoles to a range of (E)-1,4-diaryl-2-buten-1,4-diones, catalyzed by commercially available cinchonine, is described. This organocatalytic asym...

 Synonyms

Cinchonan-9-ol, (9S)-, sulfate (2:1) (salt)
(9S)-Cinchonan-9-ol sulfate (2:1)
EINECS 227-708-4
MFCD00035639
cinchonine sulfate