1713-83-3 Usage
Type of compound
Synthetic antibiotic
Function
Treats a variety of bacterial infections (respiratory tract infections, skin infections, meningitis)
Mechanism of action
Inhibits protein synthesis in bacteria
Spectrum of activity
Broad-spectrum (active against both Gram-positive and Gram-negative bacteria)
Side effects
Potential for bone marrow suppression
Precaution
Reserved for use in serious infections when other antibiotics are not effective
Usage
Should be used with caution and under the supervision of a healthcare professional due to potential toxicity
Check Digit Verification of cas no
The CAS Registry Mumber 1713-83-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1713-83:
(6*1)+(5*7)+(4*1)+(3*3)+(2*8)+(1*3)=73
73 % 10 = 3
So 1713-83-3 is a valid CAS Registry Number.
InChI:InChI=1/C3H6ClNO3/c4-1-3(6)2-5(7)8/h3,6H,1-2H2
1713-83-3Relevant articles and documents
LaCl3·7H2O-promoted regioselective ring opening of epoxides using NaNO2 in ether-water system: A facile synthesis of 2-nitroalcohols
Borah, Jagat C.,Gogoi, Siddhartha,Boruwa, Joshodeep,Barua, Nabin C.
, p. 873 - 878 (2007/10/03)
A convenient and efficient synthesis of 2-nitroalcohols has been achieved by regioselective ring opening of epoxides using LaCl3·7H 2O and NaNO2 in ether-H2O system at room temperature. The reaction afforded the corresponding products in good to excellent yields under mild conditions.
2-Amino-2-deoxytetrose derivatives. Preparation from 4,5-dihydroisoxazoles via reductive cleavage
Wade,D'Ambrosio,Price
, p. 6302 - 6308 (2007/10/03)
The 4-alkoxy-3-nitro-4,5-dihydroisoxazoles 2a,b were prepared by condensation of nitromethane and chloroacetaldehyde, protection of the resulting nitroaldol 1c, and subsequent nitrosative cyclization. Multistep replacement of the nitrogroup of 2a,b by a 2
