N,N-Dimethyl(2H)formamide

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Names

[ CAS No. ]:
2914-27-4

[ Name ]:
N,N-Dimethyl(2H)formamide

[Synonym ]:
C-deuterio-N,N-dimethyl-formamide
N,N-Dimethylformamide-D1 &N,N-Dimethylformamide-d
Formamide-d, N,N-dimethyl-
N,N-dimethylformamide-1-d
N,N-Dimethylformamide-d1
MFCD00144980
N,N-Dimethyl(H)formamide
Deuterodimethylformamid
DE795

Chemical & Physical Properties

[ Density]:
0.9±0.1 g/cm3

[ Boiling Point ]:
153.0±0.0 °C at 760 mmHg

[ Melting Point ]:
-61ºC(lit.)

[ Molecular Formula ]:
C3H6DNO

[ Molecular Weight ]:
74.100

[ Flash Point ]:
57.8±0.0 °C

[ Exact Mass ]:
74.059044

[ PSA ]:
20.31000

[ LogP ]:
-1.01

[ Vapour Pressure ]:
3.4±0.2 mmHg at 25°C

[ Index of Refraction ]:
1.396

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS07, GHS08

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H226-H312 + H332-H319-H360D

[ Precautionary Statements ]:
P201-P210-P261-P280-P308 + P313-P370 + P378

[ Hazard Codes ]:
T: Toxic;

[ Risk Phrases ]:
61-20/21-36

[ Safety Phrases ]:
53-45

[ RIDADR ]:
UN 2265 3/PG 3

Synthetic Route

Precursor & DownStream

Precursor

  • (2H2)Formaldehyde
  • Dimethylamine
  • Methyl (2H)formate
  • Dimethylamine hydrochloride

DownStream

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Haematologica 94 , 409-13, (2009)

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Large-scale 13C-flux analysis reveals distinct transcriptional control of respiratory and fermentative metabolism in Escherichia coli.

Mol. Syst. Biol. 7 , 477, (2011)

Despite our increasing topological knowledge on regulation networks in model bacteria, it is largely unknown which of the many co-occurring regulatory events actually control metabolic function and th...

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Related Compounds

  • N,N-dimethyl-2H-spiro[naphthalene-1,4'-piperidine]-4-carboxamide
  • N,N-dimethyl-2H-tetrazol-5-amine
  • 3-(dimethylamino)-N,N-dimethyl-2H-azirine-2-carboxamide
  • 1-dimethylalumanyl-N,N-dimethyl-2H-pyridin-4-amine,λ1-stibane,tritert-butylgallane,trimethylsilicon
  • 3-(dimethylamino)-N,N-dimethyl-2H-1,4-benzoxazine-2-carboxamide
  • 1-(4-acetylphenyl)sulfanyl-N,N-dimethyl-formamide
  • (3R)-3-({1-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]cyclopropyl}formamido)butanoic acid
  • (3R)-3-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]butanoic acid
  • (3R)-3-[3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]butanoic acid
  • (3R)-3-[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]butanoic acid
  • (3R)-3-[5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentanamido]butanoic acid
  • (3R)-3-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-methylbutanamido]butanoic acid
  • 2-[(3R)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)butanamido]-5-methylbenzoic acid
  • 7-[1-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cyclopropanecarbonyl]-5H,6H,7H,8H-[1,2,4]triazolo[4,3-a]pyrazine-6-carboxylic acid
  • 2-[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)but-2-enoyl]-2,3-dihydro-1H-isoindole-4-carboxylic acid
  • 3-(2-{4-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]-1H-1,2,3-triazol-1-yl}acetamido)cyclobutane-1-carboxylic acid
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