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60538-51-4

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60538-51-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60538-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,3 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60538-51:
(7*6)+(6*0)+(5*5)+(4*3)+(3*8)+(2*5)+(1*1)=114
114 % 10 = 4
So 60538-51-4 is a valid CAS Registry Number.

60538-51-4SDS

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 16-(4-Nitrobenzolsulfonimido)pentaspiro<2.0.2.0.2.0.2.0.2.1>hexadecan

1.2 Other means of identification

Product number -
Other names 16-(4-Nitrobenzolsulfonimido)pentaspiro[2.0.2.0.2.0.2.0.2.1]hexadecan

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:60538-51-4 SDS

60538-51-4Downstream Products

60538-51-4Relevant articles and documents

Polyspiranes, 5. Synthesis and Reactions of Functionalized Polyspiranes with Three- to Eight-Membered Central Ring - Polycyclopropylidenes (Rotanes)

Fitjer, Lutz

, p. 1047 - 1060 (2007/10/02)

The olefins 4, 5, and 6 have been proved to be valuable intermediates in the synthesis of functionalized polyspiranes and rotanes. Rotane (2, n = 3) and its methyl carboxylate 11 may be synthesized by way of 4, the functionalized polyspiranes 19, m = 1,2, 21, m = 0,1,2 and 1, m = 0,1,2, by way of 5.The ketones 1, m = 0,1,2 may then be transformed to the corresponding rotanes 2, n = 4,5,6.The factors controlling the pronounced regioselectivity in the cycloaddition of p-nitrobenzenesulfonyl azide to 19, m = 0,1,2, are discussed, the stepwise ring enlargement of 6 to yie ld 28 and 29 as potential precursors of 2, n = 7,8, is described.

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