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104086-26-2

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104086-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104086-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,8 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 104086-26:
(8*1)+(7*0)+(6*4)+(5*0)+(4*8)+(3*6)+(2*2)+(1*6)=92
92 % 10 = 2
So 104086-26-2 is a valid CAS Registry Number.

104086-26-2SDS

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 2,4,6-tritert-butyl-2-methoxypyran

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:104086-26-2 SDS

104086-26-2Upstream product

104086-26-2Downstream Products

104086-26-2Relevant articles and documents

1H Nuclear Magnetic Resonance Study of Methoxide Addition to Pyrylium and Thiopyrylium Cations; Heteroatom and Substituent Effects

Doddi, Giancarlo,Ercolani, Gianfranco

, p. 271 - 276 (2007/10/02)

Methoxide addition to pyrylium and thiopyrylium salts with various α-substituents (Ph or tBu) and γ-substituents (H, Me, tBu, Et3C, Ph or MeO) in methanol at -40 and 25 deg C has been studied by 1H n.m.r.The composition of the product mixtures, kinetically controlled at -40 deg C and thermodynamically controlled at 25 deg C, gives information on the factors affecting positional selectivity and the relative thermodynamic stability of the addition products (the 2H- and 4H-adduct).The methyl-substituted substrates also undergo deprotonation, to yield the corresponding anhydro-bases.Analysis of heteroatom and substituent effects on the rean course emphasizes the role of polar and steric interactions, and sheds light on the structures of the transition states.

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