Cas 336182-89-9,(2S,3S)-4-Benzyloxy-3-hydroxy-2-methyl-butyric acid (S)-3-phenyl-2-(toluene-4-sulfonylamino)-propyl ester

336182-89-9

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Basic information

Product Name: (2S,3S)-4-Benzyloxy-3-hydroxy-2-methyl-butyric acid (S)-3-phenyl-2-(toluene-4-sulfonylamino)-propyl ester
Synonyms: (2S,3S)-4-Benzyloxy-3-hydroxy-2-methyl-butyric acid (S)-3-phenyl-2-(toluene-4-sulfonylamino)-propyl ester
CAS NO:336182-89-9
Molecular Formula:
Molecular Weight: 511.639
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: (2S,3S)-4-Benzyloxy-3-hydroxy-2-methyl-butyric acid (S)-3-phenyl-2-(toluene-4-sulfonylamino)-propyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-4-Benzyloxy-3-hydroxy-2-methyl-butyric acid (S)-3-phenyl-2-(toluene-4-sulfonylamino)-propyl ester(336182-89-9)
EPA Substance Registry System: (2S,3S)-4-Benzyloxy-3-hydroxy-2-methyl-butyric acid (S)-3-phenyl-2-(toluene-4-sulfonylamino)-propyl ester(336182-89-9)

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: 336182-89-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 336182-89-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,6,1,8 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 336182-89:
(8*3)+(7*3)+(6*6)+(5*1)+(4*8)+(3*2)+(2*8)+(1*9)=149
149 % 10 = 9
So 336182-89-9 is a valid CAS Registry Number.

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336182-89-9Relevant academic research and scientific papers

Ester derived titanium enolate aldol reaction: Chelation controlled diastereoselective synthesis of syn-aldols

Ghosh, Arun K.,Kim, Jae-Hun

, p. 1227 - 1231 (2007/10/03)

A chelation controlled and highly diastereoselective synthesis of syn-aldols is described. Aldol reaction of commercially available L-phenylalaninol derived esters with a variety of bidentate oxyaldehydes proceeded with excellent syn-diastereoselectivities and isolated yields.

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