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62999-86-4

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62999-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62999-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,9 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62999-86:
(7*6)+(6*2)+(5*9)+(4*9)+(3*9)+(2*8)+(1*6)=184
184 % 10 = 4
So 62999-86-4 is a valid CAS Registry Number.

62999-86-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N,5,5-tetramethyl-1,3-dioxan-2-amine

1.2 Other means of identification

Product number -
Other names (5,5-dimethyl-[1,3]dioxan-2-yl)-dimethyl-amine

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:62999-86-4 SDS

62999-86-4Relevant articles and documents

A solution and solid state conformation of 2-diphenylphosphinoyl-1,3-dioxanes. The nature of O-C-P anomeric interactions

Mikolajczyk, Marian,Graczyk, Piotr P.,Wiecorek, Michal W.,Bujacz, Grzegorz

, p. 4209 - 4230 (2007/10/02)

Diastereoisomeric 2-diphenylphosphinoyl-1,3-dioxanes 1-4 were synthesized either via the Arbuzov reaction of isopropyl diphenylphosphinite with (1,3-dioxan-2-yl) trimethylammonium iodides or via the transacetalization reaction between 1,3-diols and diphenyl (diethoxymethyl) phosphine oxide. The latter reaction afforded less thermodynamically stable isomers of 3 and 4 in a good yield (44 and 56%, respectively). The magnitude of the anomeric effect in this system determined according to the Franck's equation was found to be 19.7 kJ/mol. Both the NMR and X-ray structural data concerning cis-4,6-dimethyl-1,3-dioxane derivatives 4 suggest that the anomeric effect could stem from several interaction, including the no-δ* C-P negative hyper-conjugation and intramolecular hydrogen bond formation.

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