Cas 1206910-97-5,(S)-N-{1-[4-(N,N''-bis(tert-butoxycarbonyl)guanidino)phenyl]ethyl}trifluoroacetamide

1206910-97-5

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Basic information

Product Name: (S)-N-{1-[4-(N,N''-bis(tert-butoxycarbonyl)guanidino)phenyl]ethyl}trifluoroacetamide
Synonyms: (S)-N-{1-[4-(N,N''-bis(tert-butoxycarbonyl)guanidino)phenyl]ethyl}trifluoroacetamide
CAS NO:1206910-97-5
Molecular Formula:
Molecular Weight: 474.48
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: (S)-N-{1-[4-(N,N''-bis(tert-butoxycarbonyl)guanidino)phenyl]ethyl}trifluoroacetamide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-{1-[4-(N,N''-bis(tert-butoxycarbonyl)guanidino)phenyl]ethyl}trifluoroacetamide(1206910-97-5)
EPA Substance Registry System: (S)-N-{1-[4-(N,N''-bis(tert-butoxycarbonyl)guanidino)phenyl]ethyl}trifluoroacetamide(1206910-97-5)

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: 1206910-97-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1206910-97-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,9,1 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1206910-97:
(9*1)+(8*2)+(7*0)+(6*6)+(5*9)+(4*1)+(3*0)+(2*9)+(1*7)=135
135 % 10 = 5
So 1206910-97-5 is a valid CAS Registry Number.

1206910-97-5Upstream product

1206910-97-5Downstream Products

1206910-98-6 (S)-1-{4-[N,N''-bis(tert-butoxycarbonyl)guanidino]phenyl}ethylamine

1206910-97-5Relevant academic research and scientific papers

Novel peptoid building blocks: Synthesis of functionalized aromatic helix-inducing submonomers

Seo, Jiwon,Barron, Annelise E.,Zuckermann, Ronald N.

, p. 492 - 495 (2010)

[Chemical equation presented] Peptoids, oligo-N-substituted glycines, can fold into well-defined helical secondary structures. The design and synthesis of new peptoid building blocks that are capable of both (a) inducing a helical secondary structure and

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