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95789-30-3

Basic Information
CAS No.: 95789-30-3
Name: Cefotiamhexetil hydrochloride
Molecular Structure:
Molecular Structure of 95789-30-3 (Cefotiamhexetil hydrochloride)
Formula: C27H39Cl2N9O7S3
Molecular Weight: 525.6281
Synonyms: 5-Thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acid, 7-(((2-amino-4-thiazolyl)acetyl)amino)-3-(((1-(2-(dimethylamino)ethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-, 1-(((cyclohexyloxy)carbonyl)oxy)ethyl ester, dihydrochloride, (6R-(6-alpha,7-beta))-;1-cyclohexyloxycarbonyloxyethyl (6R,7R)-7-[[2-(2-amino-1,3-thiazol-4-yl)acetyl]amino]-3-[[1-(2-dimethylaminoethyl)tetrazol-5-yl]sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate dihydrochloride;Cefotiam hexetil hydrochloride (JP14);Pansporin-T (TN);Pansporin-T;CTM-HE;SCE 2174;Cefotiam hexetil hydrochloride;
Density: 1.8g/cm3
Boiling Point: 980.8 °C at 760 mmHg
Flash Point: 546.9 °C
PSA: 275.83000
LogP: 4.15130
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  • Cefotiamhexetil hydrochloride

  • Casno:

    95789-30-3

    Cefotiamhexetil hydrochloride

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    1. Product advantages? High purity, all above 98.5%, no impurities after dissolution? We will test each batch to ensure quality? OEM and private brand services designed for free? Various cap colors available? We can also provide MT1 peptide powder2.

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Specification

The CAS register number of Cefotiam hexetil hydrochloride is 95789-30-3. It also can be called as (6R-(6-alpha,7-beta))-7-(((2-Amino-4-thiazolyl)acetyl)amino)-3-(((1-(2-(dimethylamino)ethyl)-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid 1-(((cyclohexyloxy)carbonyl)oxy)ethyl ester dihydrochloride and the IUPAC name about this chemical is 1-cyclohexyloxycarbonyloxyethyl (6R,7R)-7-[[2-(2-amino-1,3-thiazol-4-yl)acetyl]amino]-3-[[1-(2-dimethylaminoethyl)tetrazol-5-yl]sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate dihydrochloride. The molecular formula about this chemical is C27H37N9O7S3.2(HCl) and the molecular weight is 768.76. Classification code about this chemical are Drug / Therapeutic Agent and Reproductive Effect.

Physical properties about Cefotiam hexetil hydrochloride are: (1)ACD/LogP: 1.30; (2)# of Rule of 5 Violations: 2; (3)#H bond acceptors: 16; (4)#H bond donors: 3; (5)#Freely Rotating Bonds: 16; (6)Polar Surface Area: 275.83Å2; (7)Flash Point: 546.9 °C; (8)Enthalpy of Vaporization: 145.49 kJ/mol; (9)Boiling Point: 980.8 °C at 760 mmHg.

You can still convert the following datas into molecular structure:
(1)SMILES: Cl.O=C3N1/C(=C(\CS[C@@H]1[C@@H]3NC(=O)Cc2csc(N)n2)CSc4nnnn4CCN(C)C)C(=O)OC(C)OC(=O)OC5CCCCC5
(2)InChI: InChI=1/C27H37N9O7S3.ClH/c1-15(42-27(40)43-18-7-5-4-6-8-18)41-24(39)21-16(13-46-26-31-32-33-35(26)10-9-34(2)3)12-44-23-20(22(38)36(21)23)30-19(37)11-17-14-45-25(28)29-17;/h14-15,18,20,23H,4-13H2,1-3H3,(H2,28,29)(H,30,37);1H/t15?,20-,23-;/m1./s1
(3)InChIKey: HXCPCXZEHGGNIV-UCYVGVNQBX
(4)Std. InChI: InChI=1S/C27H37N9O7S3.ClH/c1-15(42-27(40)43-18-7-5-4-6-8-18)41-24(39)21-16(13-46-26-31-32-33-35(26)10-9-34(2)3)12-44-23-20(22(38)36(21)23)30-19(37)11-17-14-45-25(28)29-17;/h14-15,18,20,23H,4-13H2,1-3H3,(H2,28,29)(H,30,37);1H/t15?,20-,23-;/m1./s1
(5)Std. InChIKey: HXCPCXZEHGGNIV-UCYVGVNQSA-N

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LD unreported > 1gm/kg (1000mg/kg) GASTROINTESTINAL: NAUSEA OR VOMITING Gekkan Yakuji. Pharmaceuticals Monthly. Vol. 32, Pg. 1770, 1990.
mouse LD50 intraperitoneal 1150mg/kg (1150mg/kg) BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION

LIVER: OTHER CHANGES
Oyo Yakuri. Pharmacometrics. Vol. 35, Pg. 179, 1988.
mouse LD50 oral > 5gm/kg (5000mg/kg)   Drugs in Japan Vol. -, Pg. 564, 1990.
mouse LD50 subcutaneous > 2gm/kg (2000mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 35, Pg. 179, 1988.
rat LD50 intraperitoneal 1470mg/kg (1470mg/kg) BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY)

LUNGS, THORAX, OR RESPIRATION: RESPIRATORY DEPRESSION

LIVER: OTHER CHANGES
Oyo Yakuri. Pharmacometrics. Vol. 35, Pg. 179, 1988.
rat LD50 oral > 5gm/kg (5000mg/kg)   Drugs in Japan Vol. -, Pg. 564, 1990.
rat LD50 subcutaneous > 2gm/kg (2000mg/kg)   Oyo Yakuri. Pharmacometrics. Vol. 35, Pg. 179, 1988.