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1186-70-5

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1186-70-5 Usage

General Description

Methoxy-bis(dimethylamino)methane, also known as Bis[2-(dimethylamino)ethyl] ether, is a chemical compound with the formula C8H20N2O. It belongs to the class of organic compounds known as dialkyl ethers which are compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups. Its molecular weight is 160.259 g/mol. Methoxy-bis(dimethylamino)methane is generally used in research and development settings rather than in consumer products or routine manufacturing due to its chemical properties. It's essential to handle this chemical properly as it can cause skin and eye irritation and may be harmful if swallowed or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 1186-70-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1186-70:
(6*1)+(5*1)+(4*8)+(3*6)+(2*7)+(1*0)=75
75 % 10 = 5
So 1186-70-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H16N2O/c1-7(2)6(9-5)8(3)4/h6H,1-5H3

1186-70-5 Well-known Company Product Price

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  • Aldrich

  • (64875)  Bis(dimethylamino)methoxymethane  technical

  • 1186-70-5

  • 64875-10ML-F

  • 2,224.17CNY

  • Detail
  • Aldrich

  • (64875)  Bis(dimethylamino)methoxymethane  technical

  • 1186-70-5

  • 64875-50ML-F

  • 7,353.45CNY

  • Detail

1186-70-5SDS

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 1-methoxy-N,N,N',N'-tetramethylmethanediamine

1.2 Other means of identification

Product number -
Other names 1-methoxy-N,N,N',N'-tetramethylmethylenediamine

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:1186-70-5 SDS

1186-70-5Relevant articles and documents

1H Nuclear Magnetic Resonance Study of the Kinetics of the Reaction of N,N-Dialkylformamide Dimethyl Acetals with Secondary Amines

Wawer, Iwona,Osek, Jerzy

, p. 993 - 996 (1988)

Rate constants and activation parameters (ΔG, ΔH, ΔS) for the reactions of N,N-dialkylformamide dimethyl acetals with four secondary amines have been estimated by 1H n.m.r. spectroscopy.The reactions are reversible and obey a second-order kinetic equation.Substitution of one methoxy group of the amide acetal by the amine entity is found to give ester aminals which are subject to decomposition (ΔG 92-103 kJ mol-1).A transamination reaction yields a new amide acetal at higher temperatures (ΔG 115 kJ mol-1).On the basis of the kinetic data, the mechanism of these reactions is discussed.

Preparation of 1-nitroanthraquinone-2-carboxylic acid

-

, (2008/06/13)

1-Nitroanthraquinone-2-carboxylic acid of the formula I STR1 is prepared by treating novel 2-substituted 1-nitroanthraquinones of the general formula II STR2 where R is --CH=CH--R1 or --CH2 --CHO, where R1 is C1 -C5 -dialkylamino or a cyclic 5- or 6-membered amine which may contain further hetero atoms, with oxidizing agents free of heavy metal.

1H and 13C Nuclear Magnetic Resonance Identification of the Products of the Reaction of NN-Dialkylformamide Dimethyl Acetals with Secondary Amines

Wawer, Iwona,Osek, Jerzy

, p. 1669 - 1672 (2007/10/02)

Eight reactions of NN-dialkylformamide dimethyl acetals with secondary amines have been followed by means of 1H n.m.r.The reaction products were not only other amide acetals but also ester aminals and orthoamides.Therefore secondary amines exchanged the amine moiety and the methoxy group of the amide acetal.The relative concentrations of products at equilibrium have been estimated.The 13C chemical shifts for substrates and some products have been reported.

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