n,n-diethyl o-toluidine

n,n-diethyl o-toluidine structural formula

structural formula

business number 069c
molecular formula c11h17n
molecular weight 163.26
label

2-(diethylamino)toluene,

2-methyl-n,n-diethylaniline,

n,n-diethyl o-methylaniline,

(diethylamine)toluene

numbering system

cas number:606-46-2

mdl number:none

einecs number:210-119-1

rtecs number:none

brn number:none

pubchem id:none

physical property data

physical property data:
1. character:colorless or light yellow oily liquid.

2. boiling point (ºc,100.7kpa):208-209

3. solubility:soluble in ethanol and ether, insoluble in water.

4. toxicity:poisonous.

toxicological data

none yet

ecological data

3. ecological data:

1. other harmful effects: this substance may be harmful to the environment and should be harmful to water bodies. give special attention.

molecular structure data

5. molecular property data:

1, molar refractive index:54.65

2, molar volume (m3/mol): 176.7

3, isotonic specific volume (90.2k ):426.5

4, surface tension (dyne/ cm):33.9

5 polarizability (10-24cm3): 21.66

compute chemical data

1. reference value for hydrophobic parameter calculation (xlogp): none

2. number of hydrogen bond donors: 0

3. number of hydrogen bond acceptors: 1

4. number of rotatable chemical bonds: 3

5. number of tautomers: none

6. topological molecule polar surface area 3.2

7. number of heavy atoms: 12

8. surface charge: 0

9. complexity: 118

10. number of isotope atoms: 0

11. determined number of atomic stereocenters: 0

12. uncertain number of atomic stereocenters: 0

13.determined number of stereocenters of chemical bonds: 0

14. number of uncertain stereocenters of chemical bonds: 0

15. number of covalent bond units: 1

properties and stability

properties and stability:

no decomposition products may occur under normal temperatures and pressures.

storage method

1. storage

should be sealed in a cool place store in light place.

synthesis method

2. brief description of production method

from o-toluidine and ethyl bromide derived from the reaction of alkanes.

purpose

3. purpose

used in organic synthesis.

resource:allhdi.com

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/30689

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