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102741-52-6

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102741-52-6 Usage

Chemical structure

Nitro-substituted benzisoxazole derivative

Usage

Building block in the synthesis of pharmaceuticals and agrochemicals

Physical appearance

Pale yellow solid

Solubility

Insoluble in water

Melting point

High melting point (specific value not provided)

Pharmacological and biological activities

Studied for effects on the central nervous system

Functional groups

Nitro and hydroxyl groups

Versatility

Intermediate for the preparation of novel organic compounds with potential therapeutic applications

Check Digit Verification of cas no

The CAS Registry Mumber 102741-52-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,4 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102741-52:
(8*1)+(7*0)+(6*2)+(5*7)+(4*4)+(3*1)+(2*5)+(1*2)=86
86 % 10 = 6
So 102741-52-6 is a valid CAS Registry Number.

102741-52-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (6-nitro-1,2-benzoxazol-3-yl)methanol

1.2 Other means of identification

Product number -
Other names 1,2-Benzisoxazole-3-methanol,6-nitro

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:102741-52-6 SDS

102741-52-6Downstream Products

102741-52-6Relevant articles and documents

Host-Guest Interactions. The Binding Mode of 6-Nitrobenzisoxazole-3-carboxylate to Quaternary Ammonium Macrocycles

Schmidtchen, Franz P.

, p. 135 - 142 (2007/10/02)

In order to investigate the mode of substrate binding and the factors involved in catalysis by artificial host compounds, the rate augmentation of the decarboxylation of 6-nitrobenzisoxazole-3-carboxylate (4) in the presence of the non-aggregating macrocyclic quaternary ammonium salts (1)-(3) was analysed.The kinetic results indicate that (1) and (3) consisting of 27-membered macrocycles form host-guest complexes with (4) whereas (2) having 21-membered rings does not.The macrotricycle (3) is the most effective catalyst, exhibiting a temperature-independent maximum rate enhancement of 110.The rate and binding constants and their temperature dependence for (3) leads to the conclusion that (4) penetrates with the nitroaromatic moiety first into the molecular cavity of (1) and (3).This mode of association is impossible with (2) for steric reasons.The cavity of (3), however, is large enough to accommodate two substrate molecules thus allowing the observation of the rare case of co-operative substrate binding to a low molecular weight enzyme model.

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