Cas 1333506-16-3,methyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate

1333506-16-3

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Basic information

Product Name: methyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate
Synonyms: methyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate
CAS NO:1333506-16-3
Molecular Formula:
Molecular Weight: 474.513
EINECS: N/A
Product Categories: N/A

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: methyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate(1333506-16-3)
EPA Substance Registry System: methyl (2S)-2-{[(benzyloxy)carbonyl]amino}-3-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}propanoate(1333506-16-3)

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: 1333506-16-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1333506-16-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,3,5,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1333506-16:
(9*1)+(8*3)+(7*3)+(6*3)+(5*5)+(4*0)+(3*6)+(2*1)+(1*6)=123
123 % 10 = 3
So 1333506-16-3 is a valid CAS Registry Number.

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1333506-16-3Relevant academic research and scientific papers

Highly enantioselective synthesis of orthogonally protected (2S)-2,3-diaminopropanoates through catalytic phase-transfer aza-Henry reaction

Kumaraswamy, Gullapalli,Pitchaiah, Arigala

experimental part, p. 1543 - 1550 (2011/10/08)

The syntheses of enantiomer-enriched orthogonally protected different (2S)-2,3-diaminopropanoates and unnatural furyl-substituted (tert-butoxy) carbonyl (Boc) as well as (benzyloxy)carbonyl (Cbz) protected amino acid esters are accomplished by means of an

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