Salicylanilide

Modify Date: 2024-01-02 13:29:46

Salicylanilide Structure
Salicylanilide structure
Common Name Salicylanilide
CAS Number 87-17-2 Molecular Weight 213.232
Density 1.3±0.1 g/cm3 Boiling Point 294.3±23.0 °C at 760 mmHg
Molecular Formula C13H11NO2 Melting Point 136-138 °C(lit.)
MSDS Chinese USA Flash Point 131.8±22.6 °C
Symbol GHS07 GHS09
GHS07, GHS09
Signal Word Warning

 Use of Salicylanilide


Salicylanilide demonstrates a wide range of biological activities including antiviral potency which can inhibit HIV virus by targeting HIV-1 integrase or reverse transcriptase.

 Names

Name salicylanilide
Synonym More Synonyms

 Salicylanilide Biological Activity

Description Salicylanilide demonstrates a wide range of biological activities including antiviral potency which can inhibit HIV virus by targeting HIV-1 integrase or reverse transcriptase.
Related Catalog
Target

HIV-1 integrase, reverse transcriptase[1]

In Vitro Some Salicylanilides and salicylamides could inhibit HIV virus by targeting of HIV-1 integrase or reverse transcriptase. Hepatitis C virus is another virus, which can be potentially afflicted by Salicylanilides on the level of two enzymes-NS3 protease and NS5B RNA polymerase[1].
References

[1]. Krátký M, et al. Antiviral activity of substituted salicylanilides--a review. Mini Rev Med Chem. 2011 Oct;11(11):956-67.

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
Boiling Point 294.3±23.0 °C at 760 mmHg
Melting Point 136-138 °C(lit.)
Molecular Formula C13H11NO2
Molecular Weight 213.232
Flash Point 131.8±22.6 °C
Exact Mass 213.078979
PSA 49.33000
LogP 3.27
Vapour Pressure 0.0±0.6 mmHg at 25°C
Index of Refraction 1.676
Water Solubility SLIGHTLY SOLUBLE

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
VN7850000
CHEMICAL NAME :
Salicylanilide
CAS REGISTRY NUMBER :
87-17-2
BEILSTEIN REFERENCE NO. :
1108135
LAST UPDATED :
199701
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C13-H11-N-O2
MOLECULAR WEIGHT :
213.25
WISWESSER LINE NOTATION :
QR BVMR

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
2400 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
85JCAE "Prehled Prumyslove Toxikologie; Organicke Latky," Marhold, J., Prague, Czechoslovakia, Avicenum, 1986 Volume(issue)/page/year: -,663,1986
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>500 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
FRMCE8 Farmaco. (Societa Chimica Italiana, Corso Strada Nova, 86, Casella Postale 227, 27100 Pavia, Italy) V.44- 1989- Volume(issue)/page/year: 44,465,1989 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - 82917 No. of Facilities: 178 (estimated) No. of Industries: 7 No. of Occupations: 5 No. of Employees: 837 (estimated) NOES - National Occupational Exposure Survey (1983) NOES Hazard Code - 82917 No. of Facilities: 637 (estimated) No. of Industries: 10 No. of Occupations: 14 No. of Employees: 27279 (estimated) No. of Female Employees: 21161 (estimated)

 Safety Information

Symbol GHS07 GHS09
GHS07, GHS09
Signal Word Warning
Hazard Statements H315-H319-H335-H400
Precautionary Statements P261-P273-P305 + P351 + P338
Personal Protective Equipment dust mask type N95 (US);Eyeshields;Gloves
Hazard Codes Xi:Irritant;
Risk Phrases R36/37/38
Safety Phrases S26-S37/39
RIDADR UN 3077 9 / PGIII
WGK Germany 2
RTECS VN7850000
HS Code 29242995

 Synthetic Route

 Customs

HS Code 2924299090
Summary 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

 Articles27

More Articles
A closer study of peak distortions in supercritical fluid chromatography as generated by the injection.

J. Chromatogr. A. 1400 , 131-9, (2015)

In SFC the sample cannot be dissolved in the mobile phase, so it is often dissolved in pure modifier, or another liquid, sometimes resulting in serious distortions of the eluted peak profiles already ...

Application of reactive salicylanilide to viscose fabrics as antibacterial and antifungus finishing.

Int. J. Biol. Macromol. 50(1) , 273-6, (2012)

In the present study salicylanilide was reacted with 2,4,6-trichloro-1,3,5-triazine producing reactive salicylanilide at a yield of 45% according to reaction conditions set. The reactive salicylanilid...

Harmaline-resistant mutant of Methanothermobacter thermautotrophicus with a lesion in Na(+)/H(+) antiport.

Gen. Physiol. Biophys. 30 Spec No , S54-60, (2011)

A spontaneous mutant of Methanothermobacter thermautotrophicus resistant to the Na(+)/H(+) antiporter inhibitor harmaline was isolated. The Na(+)/H(+) exchange activity in the mutant cells was remarka...

 Synonyms

2-Phenylaminocarbonylphenol
Salinide
Benzamide, 2-hydroxy-N-phenyl-
Salicylanilid
2-Hydroxy-N-phenylbenzamide
Salifebrin
Ansadol
salicylamide
salicylic acid anilide
N-Phenylsalicylamide
Hyanilid
EINECS 201-727-8
2-hydroxy-N-phenyl-benzamide
Aseptolan
Salicylanilide
MFCD00002212
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