Details
Buy high quality and low price METHYLAMINOACETONITRILE 5616-32-0 now
- Molecular Formula: C3H6N2
- Molecular Weight: 70.094
- Refractive Index: 1.4190 to 1.4220
- Boiling Point: 150.2 °C at 760 mmHg
- PKA: 4.74±0.10(Predicted)
- Flash Point: 44.6 °C
- PSA: 35.82000
- Density: 0.873 g/cm3
- LogP: 0.12028
METHYLAMINOACETONITRILE(Cas 5616-32-0) Usage
|
General Description |
Methylaminoacetonitrile is an organic compound with the chemical formula C3H6N2. It is a colorless liquid that is used primarily in the production of pharmaceuticals, agrochemicals, and other organic compounds. Methylaminoacetonitrile is a versatile building block in organic synthesis, frequently used in the manufacture of a wide range of chemical products. It is also utilized in the preparation of various intermediates for pharmaceuticals and agricultural chemicals. Additionally, it is an important starting material for the synthesis of various heterocyclic compounds and is widely utilized in the field of organic chemistry as a versatile reagent for the preparation of a variety of nitrogen-containing compounds. Methylaminoacetonitrile can also be used as a solvent in various chemical reactions. |
InChI:InChI=1/C3H6N2/c1-5-3-2-4/h5H,3H2,1H3
5616-32-0 Relevant articles
High-yielding automated convergent synthesis of no-carrier-added [11C-carbonyl]-labeled amino acids using the strecker reaction
Xing, Junhao,Brooks, Allen F.,Fink, Dylan,Zhang, Huibin,Piert, Morand R.,Scott, Peter J.H.,Shao, Xia
supporting information, p. 371 - 375 (2017/02/10)
A new variant of the Strecker synthesis ...
Process for the preparation of creatine water (by machine translation)
-
Paragraph 0041; 0042, (2016/10/07)
The invention discloses a preparation me...
Microwave-assisted solvent-free intramolecular 1,3-dipolar cycloaddition reactions leading to hexahydrochromeno[4,3-b]pyrroles: scope and limitations
Pospí?il, Ji?í,Potá?ek, Milan
, p. 337 - 346 (2007/10/03)
We report the microwave-assisted solvent...
Chemistry of α-Amino Nitriles. Exploratory Experiments on Thermal Reactions of α-Amino Nitriles
Xiang, Yi-Bin,Drenkard, Susanne,Baumann, Karl,Hickey, Deirdre,Eschenmoser, Albert
, p. 2209 - 2250 (2007/10/02)
The paper extends a previously published...
5616-32-0 Process route
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-
107-16-4
glycolonitrile
-
-
74-89-5
methylamine
-
-
5616-32-0
(methylamino)acetonitrile
| Conditions | Yield |
|---|---|
|
at -10 - 50 ℃;
|
|
|
With
water;
|
|
|
With
methanol;
|
|
|
In
methanol;
|
|
|
In
water;
at 10 - 20 ℃;
for 3h;
Temperature;
Large scale;
|
-
-
50-00-0,30525-89-4,61233-19-0
formaldehyd
-
-
143-33-9,25596-52-5
sodium cyanide
-
-
593-51-1
methylamine hydrochloride
-
-
5616-32-0
(methylamino)acetonitrile
| Conditions | Yield |
|---|---|
|
In
water;
at 25 ℃;
for 0.166667h;
|
79%
|
|
at 0 ℃;
|
|
|
With
formaldehyd;
In
water;
at 0 ℃;
for 1h;
|
5616-32-0 Upstream products
-
50-00-0
formaldehyd
-
143-33-9
sodium cyanide
-
593-51-1
methylamine hydrochloride
-
107-16-4
glycolonitrile
5616-32-0 Downstream products
-
90840-21-4
N -methyl-N -phenylcarbamoyl-glycine nitrile
-
25808-34-8
N -cyanomethyl-N -methyl-N '-phenyl-benzamidine
-
1801-62-3
1,3-dimethyl-2-thioxoimidazolidin-4-one
-
13200-60-7
Sarcosine ethyl ester
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