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Spirobishexahydropyrimidine is a unique chemical compound characterized by its complex cyclic structure, which consists of two fused six-membered rings. This heterocyclic compound is notable for its spiro configuration, where two rings share a common atom, in this case, a carbon atom. The term "bishexahydropyrimidine" indicates that the compound contains two six-membered rings, each of which is a reduced form of a pyrimidine ring, meaning they contain two fewer hydrogen atoms than a fully saturated pyrimidine. These structures are of interest in organic chemistry and may have potential applications in the development of pharmaceuticals and other chemical products due to their diverse reactivity and structural properties.

4115-66-6

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4115-66-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4115-66-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,1 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4115-66:
(6*4)+(5*1)+(4*1)+(3*5)+(2*6)+(1*6)=66
66 % 10 = 6
So 4115-66-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H20N4O2/c1-9(2)5-11(14-7(16)12-9)6-10(3,4)13-8(17)15-11/h5-6H2,1-4H3,(H2,12,14,16)(H2,13,15,17)

4115-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,10,10-tetramethyl-1,3,7,9-tetrazaspiro[5.5]undecane-2,8-dione

1.2 Other means of identification

Product number -
Other names 4,4,10,10-Tetramethyl-1,3,7,9-tetrazo-spiro<5,5>undecan-2,8-dion

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:4115-66-6 SDS

4115-66-6Downstream Products

4115-66-6Relevant academic research and scientific papers

Mechanistic Studies in the Chemistry of Urea. Part 7. Reaction with Acetone and Mesityl Oxide

Butler, Anthony R.,Hussain, Ishtiaq

, p. 232 - 234 (2007/10/02)

By application of spectral methods it has been confirmed that the structure of the product of reaction between urea and acetone under acid conditions is (3).A mechanism for this reacton has been proposed.If acetone is replaced by mesityl oxide then the product is (7), rather than (6).A similar mechanism operates in this reaction.Analugous products are obtained with 1-methylurea, but 1,3-dimethylurea does not react under these conditions.

Reaction of BiCl3 with N,N'-Bis(trimethylsilyl)urea and Acetone

Georgiades, A.,Schilling, G.,Latscha, H. P.

, p. 709 - 711 (2007/10/02)

The reaction of BiCl3, N,N'-bis(trimethylsilyl)urea and acetone yields compound 1 with the formula C22H46Cl9N8O7Bi.After treatment of 1 with acetone /dimethylformamid the spirocompound 4,4,10,10-tetramethylspiro-1,3,7,9-tetrazaundecadion-2,8 (3) could be isolated.The structure of 3 is described and a reaction mechanismus is proposed. - Keywords: 4,4,10,10-Tetramethylspiro-1,3,7,9-tetrazadecadion-2,8-Bismuthtrichloride

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