Cas 882159-33-3,(4S,2'R,3'R)-3-[2'-iodo-3'-methoxy-3'-(4-benzyloxyphenyl)-propionyl]-4-(1-methylethyl)-2-oxazolidinone

882159-33-3

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Basic information

Product Name: (4S,2'R,3'R)-3-[2'-iodo-3'-methoxy-3'-(4-benzyloxyphenyl)-propionyl]-4-(1-methylethyl)-2-oxazolidinone
Synonyms: (4S,2'R,3'R)-3-[2'-iodo-3'-methoxy-3'-(4-benzyloxyphenyl)-propionyl]-4-(1-methylethyl)-2-oxazolidinone
CAS NO:882159-33-3
Molecular Formula:
Molecular Weight: 523.368
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: (4S,2'R,3'R)-3-[2'-iodo-3'-methoxy-3'-(4-benzyloxyphenyl)-propionyl]-4-(1-methylethyl)-2-oxazolidinone(CAS DataBase Reference)
NIST Chemistry Reference: (4S,2'R,3'R)-3-[2'-iodo-3'-methoxy-3'-(4-benzyloxyphenyl)-propionyl]-4-(1-methylethyl)-2-oxazolidinone(882159-33-3)
EPA Substance Registry System: (4S,2'R,3'R)-3-[2'-iodo-3'-methoxy-3'-(4-benzyloxyphenyl)-propionyl]-4-(1-methylethyl)-2-oxazolidinone(882159-33-3)

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: 882159-33-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 882159-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,1,5 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 882159-33:
(8*8)+(7*8)+(6*2)+(5*1)+(4*5)+(3*9)+(2*3)+(1*3)=193
193 % 10 = 3
So 882159-33-3 is a valid CAS Registry Number.

882159-33-3Upstream product

67-56-1 methanol

882159-33-3Downstream Products

882159-55-9 (4S,2'S,3'R)-3-[2'-azido-3'-methoxy-3'-(4-benzyloxyphenyl)-propionyl]-4-(1-methylethyl)-2-oxazolidinone

882159-33-3Relevant academic research and scientific papers

Silver(I)-promoted asymmetric halomethoxylation of chiral α,β-unsaturated carboxylic acid derivatives: Enantioselective synthesis of N-protected syn-β-methoxy-α-amino acids

Hajra, Saumen,Karmakar, Ananta,Bhowmick, Manishabrata

, p. 210 - 222 (2007/10/03)

Asymmetric halomethoxylation of chiral α,β-unsaturated carboxylic acid derivatives was performed with halogens (Br2/I 2) promoted by silver(I) salts with high regio- and anti-selectivity and moderate to good diastereoselectivity. Rea

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