1. Home
  2. Cyclopropylhydrazine dihydrochloride

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Cyclopropylhydrazine dihydrochloride

NNC1CC1.Cl.Cl Request for Quotation
Chemical Name: Cyclopropylhydrazine dihydrochloride
CAS Number: 1374652-23-9
Product Number: AG00A00R(AGN-PC-0WAJH8)
Synonyms:
MDL No:
Molecular Formula: C3H10Cl2N2
Molecular Weight: 145.0309

Identification/Properties

Computed Properties
Molecular Weight:
145.027g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
144.022g/mol
Monoisotopic Mass:
144.022g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
31.9
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Cyclopropylhydrazine dihydrochloride is a versatile chemical reagent commonly used in organic synthesis. It serves as a valuable building block in the preparation of various compounds due to its unique chemical properties and reactivity. One of the key applications of Cyclopropylhydrazine dihydrochloride is its ability to undergo diazo transfer reactions, which enable the introduction of the cyclopropyl functional group into organic molecules. This reaction is particularly useful in the synthesis of complex molecules such as natural products and pharmaceuticals. Additionally, Cyclopropylhydrazine dihydrochloride can participate in other important transformations, including cyclopropanation reactions and metal-catalyzed cross-coupling reactions, further expanding its utility in chemical synthesis.