Skip to the content
Browse the library

Diethylcarbamoyl chloride

C5H10ClNO, 135.594 g/mol. Its structure, the values that were measured, the values that were calculated, and where each one came from.

Organic — amide5 measured properties

Drawn from the SMILES. It shows how the atoms are connected — not a photograph of a molecule, and not its shape in space.

Identifiers

Molecular formula
C₅H₁₀ClNO
Molecular weight
135.594 g/mol
Exact mass
135.045092 g/mol
SMILES
CCN(CC)C(=O)Cl
InChI
InChI=1S/C5H10ClNO/c1-3-7(4-2)5(6)8/h3-4H2,1-2H3
InChIKey
OFCCYDUUBNUJIB-UHFFFAOYSA-N

Both are open without an account.

Measured properties

Values somebody obtained from a sample and published. Where two sources report the same property they are both shown, in the units each used — a disagreement between them is information, and averaging it away would be inventing a number neither one gave.

Boiling Point
186 °Cmeasured · Lide, DR (ed.). CRC Handbook of Chemistry and Physics. 81st Edition. CRC Press LLC, Boca Raton: FL 2000, p. 3-110
Melting Point
-32 °Cmeasured · Ashford, R.D. Ashford's Dictionary of Industrial Chemicals. London, England: Wavelength Publications Ltd., 1994., p. 299
Flash Point
163 - 172 °Cmeasured · reference compound database
325-342 °F (OPEN CUP)measured · Fire Protection Guide to Hazardous Materials. 12 ed. Quincy, MA: National Fire Protection Association, 1997., p. 325-36
Solubility
SOL IN WATERmeasured · National Fire Protection Association. Fire Protection Guide on Hazardous Materials. 7th ed. Boston, Mass.: National Fire Protection Association, 1978., p. 325M-72
Vapor Pressure
0.72 [mmHg]measured · reference compound database

Calculated properties

Derived from the structure rather than from a sample. These are reproducible and they are not measurements: a calculated partition coefficient and a measured one can differ by a long way, and where both exist they are listed apart on purpose.

logP
1.687calculated · chemistry engine
Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area
20.31 Ųcalculated · chemistry engine
Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors
0calculated · chemistry engine
Atoms that can donate a hydrogen bond.
H-bond acceptors
1calculated · chemistry engine
Atoms that can accept a hydrogen bond.
Rotatable bonds
2calculated · chemistry engine
Single bonds the molecule can freely twist around.
Molar refractivity
34.17 cm³/molcalculated · chemistry engine
Relates to the molecule's polarisability.
Fraction sp³ carbons
0.8calculated · chemistry engine
Share of carbon atoms with tetrahedral bonding.
QED drug-likeness
0.4169calculated · chemistry engine
Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded
8
Total atoms, hydrogen included
18
Rings
0
Aromatic rings
0
Stereocentres
0
Formal charge
0

Functional groups

  • Amide

    A carbonyl bonded directly to nitrogen.

  • Halide (C–X)

    A halogen atom attached to carbon.

Matched by structural pattern, not by a measurement.

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves Diethylcarbamoyl chloride yet.

Other names for it

No systematic name is recorded.

The sources also call it Diethylcarbamyl chloride, N,N-Diethylcarbamoyl chloride, Carbamic chloride, diethyl-, Diethylcarbamic chloride, Diethylchloroformamide, Carbamoyl chloride, diethyl-, N,N-Diethylchloroformamide, Carbamidoyl chloride, diethyl-, Diethylamid kyseliny chlormravenci, Carbamic chloride, N,N-diethyl-, N,N-Diethylcarbamyl chloride, N,N-diethylcarbamic chloride.

Structurally related

Nothing structurally close to Diethylcarbamoyl chloride has a page here yet.

Seen alongside it in reaction records

Molecules that appear in the same recorded reactions as Diethylcarbamoyl chloride. This says nothing about structure: most of them are the bases, solvents, ligands and catalysts the chemistry needed, and they are here because somebody put them in the same flask.

Where these values came from

  • chemistry engine

    structure perception

No matching record was found in the currently indexed sources (reference compound database)..

What this page does not claim

The identifiers are what the source record holds, copied rather than recomputed. Measured values are reported as their source gave them, units and all; calculated values are marked as calculated and are not measurements. Where a field is absent the page says so, because a blank cell reads as a zero and a guessed value reads as a fact.

Nothing here is a hazard assessment, a purity statement or advice about handling a sample. A flash point quoted from a safety database is a number somebody published, not a judgement by us about whether this molecule is safe for what you intend.