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Methoxymethylvinylether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63975-05-3

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63975-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63975-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,9,7 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63975-05:
(7*6)+(6*3)+(5*9)+(4*7)+(3*5)+(2*0)+(1*5)=153
153 % 10 = 3
So 63975-05-3 is a valid CAS Registry Number.

63975-05-3SDS

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 methoxymethoxyethene

1.2 Other means of identification

Product number -
Other names METHOXYMETHYLVINYLETHER

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:63975-05-3 SDS

63975-05-3Relevant academic research and scientific papers

Synthesis and structures of α-lithiated vinyl ethers

Ho, Thanh C.,Congmon, Jonathan,Zhou, Zhe,Tius, Marcus A.,Pratt, Lawrence M.

, p. 4445 - 4455 (2018/07/21)

The structures of α-lithiated vinyl ethers were explored on the basis of a combined computational and NMR study. Calculations (M06/6-31 + G(d)) on free energies of aggregate formation for a series of α-lithiated vinyl ethers indicated that the tetramer is generated preferentially in both the gas phase and THF solution, except for cyclohexylidene derivatives. (1-(Methoxymethoxy)vinyl)lithium, (2,2-difluoro-1-(methoxymethoxy)vinyl)lithium, and (1-butoxyvinyl)lithium were prepared in NMR tubes by the deprotonation of alkyl/alkoxylalkyl vinyl ethers or by the transmetalation of tin compounds. The NMR spectra of these lithium species in THF solution showed that in each species one aggregate is primarily present at 173 K, which is consistent with the preference of the tetramer.

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