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Spiro[1,3-dioxolane-2,3'-tricyclo[2.2.1.02,6]heptane], also known as 7CI, 8CI, and 9CI, is a complex organic chemical compound with the molecular formula C10H14O2. It is a spiro compound, which means it consists of two cyclic structures connected by a single carbon atom. The compound features a 1,3-dioxolane ring and a tricyclo[2.2.1.02,6]heptane ring, which are fused together. This unique structure gives the compound specific properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science. However, further research and characterization are needed to fully understand its potential uses and properties.

3213-76-1

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3213-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3213-76-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3213-76:
(6*3)+(5*2)+(4*1)+(3*3)+(2*7)+(1*6)=61
61 % 10 = 1
So 3213-76-1 is a valid CAS Registry Number.

3213-76-1SDS

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 spiro[1,2,3,4,5,6-hexahydrotricyclo[2.2.1.0<sup>2,6</sup>]heptane-7,2'-1,3-dioxolane]

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:3213-76-1 SDS

3213-76-1Downstream Products

3213-76-1Relevant academic research and scientific papers

Deamination Reactions, 48. - Decomposition of 5- and 6-Alkoxy-2-norbornanediazonium Ions

Kirmse, Wolfgang,Siegfried, Rainer,Feldmann, Georg,Schoen, Sabine,Schwarz, Johannes

, p. 477 - 484 (2007/10/02)

The aim of the present investigation was to probe the effect of 5- and 6-alkoxy substituents on the Wagner-Meerwein rearrangement of 2-norbornyl cations.The cations were generated by decomposition of the analogous diazonium ions since 6-methoxy-2-norbornyl tosylates are known to react with complete fragmentation.With the exception of 38, all 6-alkoxy-2-norbornane-diazonium ions gave acceptable yields of exo alcohols in addition to fragmentation products.These exo alcohols were formed without Wagner-Meerwein rearrangement, as indicated by the distribution of isomers or deuterium labels. 6,6-Dimethoxy-2-norbornanediazonium ions (27) showed an additional endo-6,2-OCH3 shift which was not observed with the endo-6-methoxy species 20b.In contrast, the Wagner-Meerwein rearrangement was virtually unaffected by 5-alkoxy substituents.We assume that alkoxy groups at C-6 destabilize the bridged structure of 2-norbornyl cations, as suggested by ab-inito calculations on protonated cyclopropanes.

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