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120525-82-8

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120525-82-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120525-82-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,5,2 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 120525-82:
(8*1)+(7*2)+(6*0)+(5*5)+(4*2)+(3*5)+(2*8)+(1*2)=88
88 % 10 = 8
So 120525-82-8 is a valid CAS Registry Number.

120525-82-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1,3-dinitrocyclobutane-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:120525-82-8 SDS

120525-82-8Downstream Products

120525-82-8Relevant articles and documents

Synthesis of Polynitrocyclobutane Derivatives

Archibald, T. G.,Garver, L. C.,Baum, K.,Cohen, M. C.

, p. 2869 - 2873 (1989)

The synthesis of polynitrocyclobutanes was studied.Oxidation of oximinocyclobutanes with hypochlorite followed by Zn reduction gave ethyl 3-nitrocyclobutanecarboxylate (4a), diethyl 3-nitrocyclobutane-1,1-dicarboxylate (4b), and 2,5,8,10-tetranitrodispirodecane (4d) in 20-90percent yields.Oxidation of aminocyclobutanes with m-chloroperbenzoic acid gave 1-nitrocyclobutane (4e), 1,3-dinitrocyclobutane (4f), and 2,8-dinitrodispirodecane (4c) in 20-40percent yields.Bromination of 4f gave 1,3-dibromo-1,3-dinitrocyclobutane (5).Addition of N2O4 to methyl orethyl bicyclobutane-1-carboxylates gave methyl or ethyl 1,3-dinitrocyclobutanecarboxylates (7a,b) in 17percent and 40percent yields.Oxidative nitration of nitrocyclobutanes 4a,d,e gave the corresponding gem-dinitrocyclobutanes in 15-78percent yield. 1,1,3,3-Tetranitrocyclobutane (8f) and 1,1,3-trinitrocyclobutane (11) were obtained by similar oxidative nitration of 4f or 7a,b in 20-40percent yields.Dispirane 4c was converted similarly to 5,5,10,10-tetranitrodispirodecane in 64percent yield.

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