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120383-84-8

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120383-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120383-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,3,8 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 120383-84:
(8*1)+(7*2)+(6*0)+(5*3)+(4*8)+(3*3)+(2*8)+(1*4)=98
98 % 10 = 8
So 120383-84-8 is a valid CAS Registry Number.

120383-84-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Cyclopropylmethyl)-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names o-nitrobenzylcyclopropane

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:120383-84-8 SDS

120383-84-8Relevant articles and documents

BENZYL- and 2- AND 4-NITROBENZYLCYCLOPROPANES AND THEIR REACTION WITH ORGANIC ACIDS

Fedotov, A. N.,Trofimova, E. V.,Mochalov, S. S.,Shabarov, Yu. S.

, p. 1272 - 1275 (2007/10/02)

The nitration of benzylcyclopropane and its transformations in organic acids were studied.Under the conditions of electrophilic nitration the small ring is preserved, while the ratio of the o- and p-nitrophenyl derivatives amounts to 1.1:1.The reaction of benzylcyclopropane with formic and acetic acids takes place with the addition of the fragments of the acids at the 1,2-bond of the three-carbon ring; o- and p-nitrobenzylcyclopropanes do not react with formic and acetic acids, with trifluoroacetic acid they form trifluoroacetates, and in the case of the ortho-substituted isomer nucleophilic assistance from the nitro group is observed.

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