Cas 241149-90-6,(5S,1'S)-5-[1-(benzyloxycarbonylamino)-2-phenylethyl]-3-methylenedihydro-2(3H)-furanone

241149-90-6

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Basic information

Product Name: (5S,1'S)-5-[1-(benzyloxycarbonylamino)-2-phenylethyl]-3-methylenedihydro-2(3H)-furanone
Synonyms: (5S,1'S)-5-[1-(benzyloxycarbonylamino)-2-phenylethyl]-3-methylenedihydro-2(3H)-furanone
CAS NO:241149-90-6
Molecular Formula:
Molecular Weight: 351.402
EINECS: N/A
Product Categories: N/A
Mol File: 241149-90-6.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (5S,1'S)-5-[1-(benzyloxycarbonylamino)-2-phenylethyl]-3-methylenedihydro-2(3H)-furanone(CAS DataBase Reference)
NIST Chemistry Reference: (5S,1'S)-5-[1-(benzyloxycarbonylamino)-2-phenylethyl]-3-methylenedihydro-2(3H)-furanone(241149-90-6)
EPA Substance Registry System: (5S,1'S)-5-[1-(benzyloxycarbonylamino)-2-phenylethyl]-3-methylenedihydro-2(3H)-furanone(241149-90-6)

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: 241149-90-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 241149-90-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,1,1,4 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 241149-90:
(8*2)+(7*4)+(6*1)+(5*1)+(4*4)+(3*9)+(2*9)+(1*0)=116
116 % 10 = 6
So 241149-90-6 is a valid CAS Registry Number.

241149-90-6Upstream product

241149-76-8 (2'S,3'S)-methyl 2-[3-(benzyloxycarbonylamino)-2-hydroxy-4-phenylbutyl]propenoate

241149-90-6Downstream Products

241149-90-6Relevant articles and documents

Aminoalkyl-substituted α-methylene-γ-butyrolactones from α-amino acids using an indium-mediated Barbier allyl addition

Steurer, Steffen,Podlech, Joachim

, p. 1551 - 1560 (1999)

The indium-mediated reaction of Z-protected α-amino aldehydes 1-6 with 2-(bromomethyl)acrylates 8/9 in aqueous solvents has been investigated. The preference for the formation of syn-configured homoallyl alcohols 10-16 (diastereoselectivities ranging from

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