Cas 1421864-92-7,(3R,4S)-7-[(tert-butyldimethylsilyl)oxy]-3-methylhept-1-en-4-yl p-nitrobenzoate

1421864-92-7

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Basic information

Product Name: (3R,4S)-7-[(tert-butyldimethylsilyl)oxy]-3-methylhept-1-en-4-yl p-nitrobenzoate
Synonyms: (3R,4S)-7-[(tert-butyldimethylsilyl)oxy]-3-methylhept-1-en-4-yl p-nitrobenzoate
CAS NO:1421864-92-7
Molecular Formula:
Molecular Weight: 407.582
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: (3R,4S)-7-[(tert-butyldimethylsilyl)oxy]-3-methylhept-1-en-4-yl p-nitrobenzoate(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S)-7-[(tert-butyldimethylsilyl)oxy]-3-methylhept-1-en-4-yl p-nitrobenzoate(1421864-92-7)
EPA Substance Registry System: (3R,4S)-7-[(tert-butyldimethylsilyl)oxy]-3-methylhept-1-en-4-yl p-nitrobenzoate(1421864-92-7)

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: 1421864-92-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1421864-92-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,8,6 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1421864-92:
(9*1)+(8*4)+(7*2)+(6*1)+(5*8)+(4*6)+(3*4)+(2*9)+(1*2)=157
157 % 10 = 7
So 1421864-92-7 is a valid CAS Registry Number.

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1421864-92-7Relevant academic research and scientific papers

Stereo- and regioselective synthesis of 2-amino-3,5-diols via stereospecific crotyl transfer and regioselective aminohydroxylation

McDonald, Frank E.,Pereira, Claney L.

, p. 3639 - 3648 (2012)

A short synthesis of 2-amino-3,5-diols is described, including the all-S isomer enigmol, a synthetic anticancer compound inspired by the structure of fumonisin B The synthetic route features 1) stereospecific crotyl transfer to tetradecanal via pericyclic

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