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1-chloro-3-nitro-propan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1713-83-3

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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

1713-83-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-nitropropan-2-ol

1.2 Other means of identification

Product number -
Other names 1-Chlor-3-nitropropan-2-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1713-83-3 SDS

1713-83-3Relevant academic research and scientific papers

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.

Synthesis of 2-nitroalcohols by regioselective ring opening of epoxides with MgSO4/MeOH/NaNO2 system: A short synthesis of immunosuppressive agent FTY-720

Kalita,Barua,Bezbarua,Bez

, p. 1411 - 1414 (2007/10/03)

It has been demonstrated that a variety of epoxides can easily be opened with a system consisting of MgSO4/MeOH/NaNO2 giving the corresponding 2-nitroalcohols in excellent yields. This strategy has been applied to achieve a short synthesis of Immunosuppressive Agent FTY - 720.

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

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