Cas 1260108-98-2,ditert-butyl (R)-1-(1-ethoxy-2-fluoro-1,3-dioxo-3-p-tolylpropan-2-yl)hydrazine-1,2-dicarboxylate

1260108-98-2

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Basic information

Product Name: ditert-butyl (R)-1-(1-ethoxy-2-fluoro-1,3-dioxo-3-p-tolylpropan-2-yl)hydrazine-1,2-dicarboxylate
Synonyms: ditert-butyl (R)-1-(1-ethoxy-2-fluoro-1,3-dioxo-3-p-tolylpropan-2-yl)hydrazine-1,2-dicarboxylate
CAS NO:1260108-98-2
Molecular Formula:
Molecular Weight: 454.496
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: ditert-butyl (R)-1-(1-ethoxy-2-fluoro-1,3-dioxo-3-p-tolylpropan-2-yl)hydrazine-1,2-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ditert-butyl (R)-1-(1-ethoxy-2-fluoro-1,3-dioxo-3-p-tolylpropan-2-yl)hydrazine-1,2-dicarboxylate(1260108-98-2)
EPA Substance Registry System: ditert-butyl (R)-1-(1-ethoxy-2-fluoro-1,3-dioxo-3-p-tolylpropan-2-yl)hydrazine-1,2-dicarboxylate(1260108-98-2)

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: 1260108-98-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1260108-98-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,1,0 and 8 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1260108-98:
(9*1)+(8*2)+(7*6)+(6*0)+(5*1)+(4*0)+(3*8)+(2*9)+(1*8)=122
122 % 10 = 2
So 1260108-98-2 is a valid CAS Registry Number.

1260108-98-2Upstream product

1260108-98-2Downstream Products

1260108-98-2Relevant academic research and scientific papers

Highly enantioselective amination reactions of fluorinated keto esters catalyzed by novel chiral guanidines derived from cinchona alkaloids

Han, Xiao,Zhong, Fangrui,Lu, Yixin

, p. 2778 - 2782 (2010)

Novel Cinchona alkaloid-derived guanidines catalyze stereoselective aminations of fluorinated keto esters, affording products with fluorine-containing quaternary stereogenic centers in excellent yields and with moderate to high enantioselectivities.

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