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2-Methyl-1,3,6-trioxocane is an organic compound with the molecular formula C4H6O3. It is a cyclic ether that consists of a four-carbon ring with three oxygen atoms and one methyl group attached to the second carbon. This chemical is known for its potential use as a fuel additive or as a precursor in the synthesis of other organic compounds. It is characterized by its ability to release a significant amount of energy when combusted, which makes it an interesting candidate for applications in the energy sector. However, it is important to note that the handling, storage, and use of 2-methyl-1,3,6-trioxocane should be done with caution due to its reactivity and potential hazards.

2781-01-3

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2781-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2781-01-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,8 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2781-01:
(6*2)+(5*7)+(4*8)+(3*1)+(2*0)+(1*1)=83
83 % 10 = 3
So 2781-01-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H12O3/c1-6-8-4-2-7-3-5-9-6/h6H,2-5H2,1H3

2781-01-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-1,3,6-trioxocane

1.2 Other means of identification

Product number -
Other names Acetaldehyde,cyclic oxydiethylene acetal

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:2781-01-3 SDS

2781-01-3Relevant academic research and scientific papers

Compounds Related to Acyclovir. IX. Synthesis of 7-Hydroxy-2,5-Dioxaheptyl Derivatives of Nucleic Bases

Smirnov, I. P.,Tsilevich, T. L.,Kochetkova, S. V.,Gottikh, B. P.,Shchaveleva, I. L.,Florent'ev, V. L.

, p. 684 - 688 (2007/10/03)

7-Hydroxy-2,5-dioxaheptyl and racemic 7-hydroxy-1-methyl-2,5-dioxaheptyl derivatives of uracil, thymine, cytosine, adenine, guanine, and 1,2,4-triazole-3-carboxamide were synthesized using 7-acetyloxy-1-chlor-2,5-dioxaheptane and 8-acetyloxy-2-chlor-3,6-d

Crown Ether Acetals: Synthesis and Characterisation of a Family of Novel Oxygen Macrocyclic Compounds

Gold, Victor,,Sghibartz, Cristian M.

, p. 453 - 458 (2007/10/02)

The synthesis of cyclic acetals containing a repetitive -CH2CH2O- grouping within the ring is described.Compounds with rings of up to thirty-four members and with one or two acetal groups have been prepared and characterised by their 1H and 13C n.m.r. spectra, the amount of acetaldehyde released on hydrolysis, and their molecular weights.The general formulae of the new compounds are CH3CH(OCH2CH2)nO with n = 2-6; CH3CH(OCH2CH2)nOCH(CH3)(OCH2CH2)nO, with n = 2-5; RCH(OCH2CH2)2O with R = Pr, Pri, Ph; and C6H4O(CH2CH2O)nCH(CH3)(OCH2CH2)nO, with n = 0, 1, 2.As precursors for compounds related to the last of these series, the new open-chain dichloroacetals CH3CH2, with n = 2, 3 were prepared.Rate constants for the acid catalysed hydrolysis of some of the new acetals are reported.

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