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CasNo: 693-13-0
MF: C7H14N2
Appearance: Colorless to pale yellow liquid
The invention discloses a process method...
The invention relates to a method for sy...
The invention belongs to the technical f...
A process featuring a sequential multico...
N1-cyano-N2,N3-diisopropylguanidine
1,3-diisopropylurea
diisopropyl-carbodiimide
Conditions | Yield |
---|---|
With tert-butylhypochlorite; potassium tert-butylate; In tetrachloromethane; at -75 ℃; for 3h;
|
10% 15% |
1,3-diisopropylurea
triphenylphosphine
Triphenylphosphine oxide
diisopropyl-carbodiimide
Conditions | Yield |
---|---|
With aluminum oxide; In dichloromethane; constant current electrolysis;
|
92% |
With aluminum oxide; constant current electrolysis;
|
92% |
N,N'-diisopropylhydrazine
1,3-diisopropylthiourea
1,3-diisopropylurea
triphenylphosphine
N,N’-diisopropyl-O-isopropylisourea
N,N’-diisopropyl-O-methylisourea
1-isopropyl-4-isopropylimino-3,3-dimethyl-azetidin-2-one
ethyl N,N′-diisopropylcarbamimidate