<生产厂家价格>

弱金鸡纳碱硫酸盐二水合物

弱金鸡纳碱硫酸盐二水合物用途

用于生化研究。

弱金鸡纳碱硫酸盐二水合物名称

[ CAS 号 ]:
5949-16-6

[ 中文名 ]:
弱金鸡纳碱硫酸

[ 英文名 ]:
(9S)-Cinchonan-9-ol sulfate (2:1)

[中文别名 ]:

[英文别名 ]:

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

弱金鸡纳碱硫酸盐二水合物物理化学性质

[ 密度 ]:
1.61g/cm3

[ 沸点 ]:
169 °C(lit.)

[ 熔点 ]:
38-40 °C(lit.)

[ 分子式 ]:
C₃₈H₄₆N₄O₆S

[ 分子量 ]:
686.860

[ 闪点 ]:
148 °F

[ 精确质量 ]:
686.313782

[ PSA ]:
155.70000

[ LogP ]:
6.63300

[ 外观性状 ]:
固体;White to Light yellow powder to crystal

[ 折射率 ]:
1.717

[ 储存条件 ]:
避免光

弱金鸡纳碱硫酸盐二水合物MSDS

详细MSDS(安全技术说明书)

弱金鸡纳碱硫酸盐二水合物毒性和生态

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

弱金鸡纳碱硫酸盐二水合物安全信息

[ 危害码 (欧洲) ]:
Xi

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
26-36

[ 危险品运输编码 ]:
1544

[ WGK德国 ]:
3

[ RTECS号 ]:
GD3800000

[ 包装等级 ]:
III

[ 危险类别 ]:
6.1(b)

弱金鸡纳碱硫酸盐二水合物文献

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...

更多文献