ChemicalBook > CAS DataBase List > 3-azabicyclo[3.1.0]hexane

3-azabicyclo[3.1.0]hexane

Product Name
3-azabicyclo[3.1.0]hexane
CAS No.
285-59-6
Chemical Name
3-azabicyclo[3.1.0]hexane
Synonyms
UKRORGSYN-BB BBV-265866;3-azabicyclo[3.1.0]hexane;3-Azabicyclo[3.1.0]hexane (8CI, 9CI, ACI)
CBNumber
CB51562340
Molecular Formula
C5H9N
Formula Weight
83.13
MOL File
285-59-6.mol
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H320Causes eye irritation

H335May cause respiratory irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P330Rinse mouth.

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N-Bromosuccinimide Price

TRC
Product number
A965770
Product name
3-Azabicyclo[3.1.0]hexane
Packaging
50mg
Price
$130
Updated
2021/12/16
TRC
Product number
A965770
Product name
3-Azabicyclo[3.1.0]hexane
Packaging
100mg
Price
$200
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0110640
Product name
3-AZABICYCLO[3.1.0]HEXANE
Purity
95.00%
Packaging
1G
Price
$1216.37
Updated
2021/12/16
Matrix Scientific
Product number
123669
Product name
3-Azabicyclo[3.1.0]hexane
Purity
95+%
Packaging
1g
Price
$1552
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0110640
Product name
3-AZABICYCLO[3.1.0]HEXANE
Purity
95.00%
Packaging
2.5G
Price
$1906.96
Updated
2021/12/16
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3-azabicyclo[3.1.0]hexane Chemical Properties,Usage,Production

Uses

3-Azabicyclo[3.1.0]hexane is a key structural feature found in a wide range of biologically active natural products, drugs, and agrochemicals.

Synthesis

3-azabicyclo[3.1.0]hexane synthesis: 1-Chlorocyclopropyl p-tolyl sulfoxides with an N,N-disubstituted aminomethyl group on the cyclopropane ring were prepared from dichloromethyl p-tolyl sulfoxide, α,β-unsaturated carboxylic acid esters, primary amines, and alkyl halides. Treatment of the sulfoxides with i-PrMgCl generated cyclopropylmagnesium carbenoids, which were inserted into an intramolecular C–H bond adjacent to a nitrogen atom to give 3-azabicyclo[3.1.0]hexane in yields of up to 94%.

3-azabicyclo[3.1.0]hexane Preparation Products And Raw materials

Raw materials

Preparation Products

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3-azabicyclo[3.1.0]hexane Suppliers

China 29 Ukraine 1 United States 4 Global 34
UkrOrgSynthesis Ltd.
Tel
--
Fax
--
Email
y.barysheva@ukrorgsynth.com
Country
Ukraine
ProdList
6230
Advantage
38

285-59-6, 3-azabicyclo[3.1.0]hexaneRelated Search:

Procymidone TROVAFLOXACIN Alatrofloxacin 3-AZABICYCLO[3.1.0]HEXANE-2,4-DIONE ETHYL 2,4-DIOXO-3-[3-(TRIFLUOROMETHYL)PHENYL]-3-AZABICYCLO[3.1.0]HEXANE-6-CARBOXYLATE Duocarmycin A ADOZELESIN BICIFADINE 3-BENZYL-3-AZABICYCLO[3.1.0]HEXANE-2,4-DIONE Ciproximide 3-(3,5-difluorophenyl)-3-azabicyclo[3.1.0]hexane-2,4-dione AKOS 90874 3-(4-pyridinylmethyl)-3-azabicyclo[3.1.0]hexane-2,4-dione indolizomycin 3-[2-(4-fluorophenyl)-2-oxoethyl]-3-azabicyclo[3.1.0]hexane-2,4-dione TROVAFLOXACIN MESILATE ETHYL 2,4-DIOXO-3-PHENYL-3-AZABICYCLO[3.1.0]HEXANE-6-CARBOXYLATE 1H-Indole-2-carboxamide, N-(2-((4,5,8,8a-tetrahydro-7-methyl-4-oxocycl opropa(C)pyrrolo(3,2-e)indol-2(1H)-yl)carbonyl)-1H-indol-5-yl)-, (+-)-

  • 3-azabicyclo[3.1.0]hexane
  • UKRORGSYN-BB BBV-265866
  • 3-Azabicyclo[3.1.0]hexane (8CI, 9CI, ACI)
  • 285-59-6
  • CHIRAL CHEMICALS