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134142-29-3

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134142-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134142-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,1,4 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 134142-29:
(8*1)+(7*3)+(6*4)+(5*1)+(4*4)+(3*2)+(2*2)+(1*9)=93
93 % 10 = 3
So 134142-29-3 is a valid CAS Registry Number.

134142-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name exo-3-methyl-5-phenyl-2-oxo-3,4-diazabicyclo[4.1.0]hept-4-ene-7-spiro-1'-indane

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:134142-29-3 SDS

134142-29-3Downstream Products

134142-29-3Relevant articles and documents

1,3-Dipolar Cycloaddition of 2-Diazoalkanes to Pyridazin-3(2H)-one Derivatives. The Formation of 3H-Pyrazolopyridazin-4(5H)-one and 3H-Pyrazolopyridazin-7(6H)-one Derivatives

Stimac, Anton,Stanovnik, Branko,Tisler, Miha

, p. 417 - 423 (2007/10/02)

1,3-Dipolar cycloadditions of diazoalkanes to pyridazin-3(2H)-ones 1-7 and pyridazin-3(2H)-thiones 8 and 9 are regioselective producing 3H-pyrazolopyridazin-4(5H)-ones 15-19, 27-29 and 34-38 as the major products.In some instances, the isomeric 3H-pyrazolopyridazin-7(6H)-ones, such as 20 and 23 were isolated as the minor products.From 3 and 6 the primary 3a,7a-dihydro cycloadducts 25 and 26, and rearranged 1,2-dihydro intermediate 31 were isolated.From 10 and 1-diazoindane the isomeric exo- and endo-spiro products 39 and 40 were formed.

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