Cas 182204-97-3,[(S)-1-((4R,5R)-5-Isobutyl-2,2-dioxo-2λ<sup>6</sup>-[1,3,2]dioxathiolan-4-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester

182204-97-3

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Basic information

Product Name: [(S)-1-((4R,5R)-5-Isobutyl-2,2-dioxo-2λ⁶-[1,3,2]dioxathiolan-4-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester
Synonyms: [(S)-1-((4R,5R)-5-Isobutyl-2,2-dioxo-2λ⁶-[1,3,2]dioxathiolan-4-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester
CAS NO:182204-97-3
Molecular Formula:
Molecular Weight: 399.508
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)-1-((4R,5R)-5-Isobutyl-2,2-dioxo-2λ⁶-[1,3,2]dioxathiolan-4-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-((4R,5R)-5-Isobutyl-2,2-dioxo-2λ⁶-[1,3,2]dioxathiolan-4-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester(182204-97-3)
EPA Substance Registry System: [(S)-1-((4R,5R)-5-Isobutyl-2,2-dioxo-2λ⁶-[1,3,2]dioxathiolan-4-yl)-2-phenyl-ethyl]-carbamic acid tert-butyl ester(182204-97-3)

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: 182204-97-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 182204-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,2,0 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 182204-97:
(8*1)+(7*8)+(6*2)+(5*2)+(4*0)+(3*4)+(2*9)+(1*7)=123
123 % 10 = 3
So 182204-97-3 is a valid CAS Registry Number.

182204-97-3Upstream product

154799-20-9 (2S,3R,4R)-2--6-methyl-1-phenylheptane-3,4-diol

182204-97-3Downstream Products

182204-97-3Relevant academic research and scientific papers

Selective inversion of the proximal or distal hydroxyl groups in syn,syn-3-[N-(alkoxycarbonyl)ammo] 1,2-diols via cyclic sulfates

Kemp, Scott J.,Bao, Jianming,Pedersen, Steven F.

, p. 7162 - 7167 (2007/10/03)

The formation of cyclic sulfates (4) from syn, syn-3-[N-(benzyloxycarbonyl)amino] 1,2-diols provides a common intermediate to access other diastereomers via two inversion procedures. Thermolysis of the cyclic sulfates in acetonitrile normally leads to inversion of the distal hydroxyl group to form a 1,3-oxazin-2-one (6). Catalytic hydrogenation of the cyclic sulfates under basic conditions (NEt3) results in inversion at the proximal hydroxyl group to form a 1,3-oxazolidin-2-one (5).

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