Cas 1026035-32-4,3-(4-tert-butoxy-phenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-thiopropionic acid S-pyridin-2-yl ester

1026035-32-4

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Basic information

Product Name: 3-(4-tert-butoxy-phenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-thiopropionic acid S-pyridin-2-yl ester
Synonyms: 3-(4-tert-butoxy-phenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-thiopropionic acid S-pyridin-2-yl ester
CAS NO:1026035-32-4
Molecular Formula:
Molecular Weight: 552.694
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: 3-(4-tert-butoxy-phenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-thiopropionic acid S-pyridin-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-tert-butoxy-phenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-thiopropionic acid S-pyridin-2-yl ester(1026035-32-4)
EPA Substance Registry System: 3-(4-tert-butoxy-phenyl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-thiopropionic acid S-pyridin-2-yl ester(1026035-32-4)

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: 1026035-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1026035-32-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,0,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1026035-32:
(9*1)+(8*0)+(7*2)+(6*6)+(5*0)+(4*3)+(3*5)+(2*3)+(1*2)=94
94 % 10 = 4
So 1026035-32-4 is a valid CAS Registry Number.

1026035-32-4Upstream product

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1026035-32-4Relevant academic research and scientific papers

Synthesis of Fmoc-protected amino ketones bearing tert-butyl based side-chain protecting groups

Vázquez, Jesús,Albericio, Fernando

, p. 7499 - 7502 (2002)

A variety of Fmoc-protected amino ketones have been prepared in good yields from amino acids by their transformation into thioesters of 2-mercaptopyridine and reaction of the resulting products with dialkylcuprates.

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