Cas 170997-08-7,N-(Benzyloxycarbonyl)alanine-N'-<<(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl>methyl>amide

170997-08-7

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Basic information

Product Name: N-(Benzyloxycarbonyl)alanine-N'-<<(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl>methyl>amide
Synonyms: N-(Benzyloxycarbonyl)alanine-N'-<<(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl>methyl>amide
CAS NO:170997-08-7
Molecular Formula:
Molecular Weight: 458.314
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: N-(Benzyloxycarbonyl)alanine-N'-<<(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl>methyl>amide(CAS DataBase Reference)
NIST Chemistry Reference: N-(Benzyloxycarbonyl)alanine-N'-<<(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl>methyl>amide(170997-08-7)
EPA Substance Registry System: N-(Benzyloxycarbonyl)alanine-N'-<<(5S)-2,2-bis(trifluoromethyl)-4-oxo-1,3-dioxolan-5-yl>methyl>amide(170997-08-7)

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: 170997-08-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 170997-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,0,9,9 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 170997-08:
(8*1)+(7*7)+(6*0)+(5*9)+(4*9)+(3*7)+(2*0)+(1*8)=167
167 % 10 = 7
So 170997-08-7 is a valid CAS Registry Number.

170997-08-7Upstream product

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170997-08-7Relevant academic research and scientific papers

New Efficient Strategy for the Incorporation of (S)-Isoserine into Peptides

Burger, Klaus,Windeisen, Elisabeth,Pires, Raul

, p. 7641 - 7645 (2007/10/03)

A new efficient synthesis of (S)-isoserine derivatives from (S)-malic acid using hexafluoroacetone as protecting and activating reagent is described.Via this route (S)-isoserine is obtained as mono- and diactivated species suitable for the incorporation of isoserine into the N- and C-terminal positions of peptides.

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