Cas 34891-13-9,Bicyclo[3.1.0]hexane, 1-bromo-2-methyl-, (1-alpha-,2-ba-,5-alpha-)- (9CI)

34891-13-9

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Basic information

Product Name: Bicyclo[3.1.0]hexane, 1-bromo-2-methyl-, (1-alpha-,2-ba-,5-alpha-)- (9CI)
Synonyms: Bicyclo[3.1.0]hexane,1-bromo-2-methyl-,(1-alpha-,2-bta-,5-alpha-)-(9CI);Bicyclo[3.1.0]hexane, 1-bromo-2-methyl-, (1-alpha-,2-ba-,5-alpha-)- (9CI)
CAS NO:34891-13-9
Molecular Formula: C7H11Br
Molecular Weight: 175.06624
EINECS: N/A
Product Categories: CYCLOPENTANE
Mol File: 34891-13-9.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Bicyclo[3.1.0]hexane, 1-bromo-2-methyl-, (1-alpha-,2-ba-,5-alpha-)- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: Bicyclo[3.1.0]hexane, 1-bromo-2-methyl-, (1-alpha-,2-ba-,5-alpha-)- (9CI)(34891-13-9)
EPA Substance Registry System: Bicyclo[3.1.0]hexane, 1-bromo-2-methyl-, (1-alpha-,2-ba-,5-alpha-)- (9CI)(34891-13-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 34891-13-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 34891-13-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,9 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 34891-13:
(7*3)+(6*4)+(5*8)+(4*9)+(3*1)+(2*1)+(1*3)=129
129 % 10 = 9
So 34891-13-9 is a valid CAS Registry Number.

34891-13-9Upstream product

32264-69-0 1,1-dibromo-2-(3-butenyl) cyclopropane

34891-13-9Downstream Products

34891-13-9Relevant academic research and scientific papers

CYCLOPROPYL HALIDES. ELECTRON TRANSFER IN THE LITHIUM ALUMINIUM HYDRIDE REDUCTION OF GEM-DIBROMO AND MONOBROMOCYCLOPROPANES.

McKinney, Michael A.,Anderson, Steve W.,Keyes, Michael,Schmidt, Ronald

, p. 3443 - 3446 (2007/10/02)

The stereochemistry of reduction of mixtures of r-1-bromo-1-deuterio-c- and t-2-phenylcyclopropane and the cyclized products from 1,1-dibromo-2-(3-butenyl) cyclopropane upon reduction with lithium aluminium hydride give evidence of a configurationally equilibrated cyclopropyl radical as a reaction intermediate.

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