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(R)-4-Benzyl-2-oxazolidinone

CAS No.: 102029-44-7

Chemical Name:: (R)-4-Benzyl-2-oxazolidinone

Synonyms: (R)-4-(PHENYLMETHYL)-2-OXAZOLIDINONE;RBOX;4-benzyl-2-0xazolidinone;(4R)-Phenylmethyl-2-oxazolidinone;R-BOZ;MLS00;TB-2044;TL806371;-2-oxazoL;(R)-4-BenzyL

CBNumber:: CB7852611

Molecular Formula:: C10H11NO2

Molecular Weight:: 177.2

MOL File:: 102029-44-7.mol

MSDS File:: SDS

Modify Date:: 2024/3/28 14:27:36

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(R)-4-Benzyl-2-oxazolidinone Properties

Melting point	88-90 °C
alpha	62 º (C=1, CHCl3)
Boiling point	309.12°C (rough estimate)
Density	1.1607 (rough estimate)
refractive index	14.5 ° (C=5, MeOH)
storage temp.	Inert atmosphere,Room Temperature
solubility	Chloroform (Slightly)
form	Crystalline Powder
pka	12.78±0.40(Predicted)
color	White to almost white
optical activity	[α]18/D +64°, c = 1 in chloroform
Water Solubility	Insoluble in water. Soluble in Chloroform.
Sensitive	Hygroscopic
BRN	4782551
CAS DataBase Reference	102029-44-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)

GHS07

Signal word

Warning

Hazard statements

H320

Precautionary statements

P264-P305+P351+P338+P337+P313

Hazard Codes

Risk Statements

36/37/38

Safety Statements

22-24/25-36-26

WGK Germany

3-10

HS Code

29349990

NFPA 704

	1
2		0

(R)-4-Benzyl-2-oxazolidinone price More Price(4)

Manufacturer	Product number	Product description	CAS number	Packaging	Price	Updated	Buy
Sigma-Aldrich(India)	300977	(R)-4-Benzyl-2-oxazolidinone 99%	102029-44-7	5G	₹6018.7	2022-06-14	Buy
Sigma-Aldrich(India)	300977	(R)-4-Benzyl-2-oxazolidinone 99%	102029-44-7	25G	₹31922.93	2022-06-14	Buy
TCI Chemicals (India)	B1786	(R)-4-Benzyl-2-oxazolidinone min. 98.0 %	102029-44-7	5G	₹3400	2022-05-26	Buy
TCI Chemicals (India)	B1786	(R)-4-Benzyl-2-oxazolidinone min. 98.0 %	102029-44-7	25G	₹14900	2022-05-26	Buy

Product number	Packaging	Price	Buy
300977	5G	₹6018.7	Buy
300977	25G	₹31922.93	Buy
B1786	5G	₹3400	Buy
B1786	25G	₹14900	Buy

(R)-4-Benzyl-2-oxazolidinone Chemical Properties,Uses,Production

Description

(R)-4-Benzyl-2-oxazolidinone is a derivative of oxazolidinone. It can be used in the preparation of enantiopure carbocyclic nucleosides, which act as a HIV protease inhibitor. It can also be used as a chiral auxiliary in the enantioselective synthesis of (2R, 2′S)-erythro-methylphenidate, beta-lactams and alpha-amino acids. Its end product includes asymmetric single isomeric drugs such as antitumor, anesthetic and entipasmodic products.

Chemical Properties

white to light yellow crystal powde

References

http://www.sigmaaldrich.com/catalog/product/aldrich/300977? lang=en®ion=US
https://www.alfa.com/en/catalog/A16770/ Shieh, Wen Chung, et al. "Synthesis of enantiomerically enriched 4- piperidinylglycine." US, US 6670477B2. 2003.

(R)-4-Benzyl-2-oxazolidinone Preparation Products And Raw materials

Raw materials

Preparation Products

(R)-4-Benzyl-2-oxazolidinone Suppliers

Global( 545)Suppliers

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Supplier	Advantage
GLR Innovations	58
JSK Chemicals	58
ALS INDIA LIFE SCIENCES	58
A.J Chemicals	58
CLEARSYNTH LABS LTD.	58
TCI Chemicals (India) Pvt. Ltd.	58
Pharmaffiliates Analytics and Synthetics P. Ltd	58
Naath Industries	58
VASIN BIO LIFE SCIENCES PVT LTD	58
Pharma Affiliates	58

(R)-4-Benzyl-2-oxazolidinone Spectrum

(R)-4-Benzyl-2-oxazolidinone(102029-44-7)MS (R)-4-Benzyl-2-oxazolidinone(102029-44-7)¹HNMR (R)-4-Benzyl-2-oxazolidinone(102029-44-7)¹³CNMR (R)-4-Benzyl-2-oxazolidinone(102029-44-7)IR1 (R)-4-Benzyl-2-oxazolidinone(102029-44-7)IR2 (R)-4-Benzyl-2-oxazolidinone(102029-44-7)Raman

102029-44-7((R)-4-Benzyl-2-oxazolidinone)Related Search:

(-)-4-Benzyl-2-oxazolidinone,(S)-(-)-4-BENZYL-2-OXAZOLIDINONE,(S)-4-BENZYL-2-OXAZOLIDINONE,4-(S)-Benzyl-2-oxazolidinone,(S)-4-Benzyl-2-oxazolidinone, >99% ee (S)-(+)-4-Phenyl-2-oxazolidinone (N-CHLOROACETYL)-(4S)-BENZYL-2-OXAZOLIDINONE N-PROPIONYL-(4R)-BENZYL-2-OXAZOLIDINONE,N-3-PROPIONYL-(4R)-BENZYL-2-OXAZOLIDINONE (S)-4-(4'-Nitrobenzyl)-1,3-oxazolidine-2-one

(R)-(+)-5,5-DIPHENYL-4-BENZYL-2-OXAZOLIDINONE (R)-4-Benzyl-2-oxazolidinone 4-(4-Hydrazinobenzyl)-2-oxazolidinone N-PROPIONYL-(4S)-BENZYL-2-OXAZOLIDINONE,N-3-PROPIONYL-(4S)-BENZYL-2-OXAZOLIDINONE S/R-4-BENZYL-2-OXAZOLIDINONE

2-Oxazolidone (R)-4-(4-AMINOMETHYL-BENZYL)-OXAZOLIDIN-2-ONE (3S,4R)-4-BENZYL-3-(3-METHYLPENTANOYL)-OXAZOLIDIN-2-ONE (N-ACETYL)-(4R)-BENZYL-2-OXAZOLIDINONE Z-D-Phenylalanine N-carboxyanhydride

(R)-4-BENZYL-OXAZOLIDINE-2,5-DIONE (R)-4-BENZYL-3-(3-CYCLOPENTYL-PROPIONYL)-OXAZOLIDIN-2-ONE (R)-4-BENZYL-3-(3-CYCLOPROPYL-PROPIONYL)-OXAZOLIDIN-2-ONE

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(R)-4-BENZYL-2-OXAZOLIDINONE HPLC 99+% (R)-4-BENZYL-2-OXAZOLIDINONE 98.0% (4R)-4-(Phenylmethyl)-1,3-oxazolidin-2-one (4R)-4-(Phenylmethyl)-2-oxazolidinone (4R)-Benzyloxazolidin-2-one (R)-(+)-4-BENZYL-2-OXAZOLIDINONE FOR SYN (R)-(+)-4-Benzyl-2-oxazolidinone≥ 99.5% (HPLC, Chiral purity) R-BOZ (4R)-4-Benzyl-2-oxo-1,3-oxazolidine, (4R)-4-(Phenylmethyl)-1,3-oxazolidin-2-one (R)-4-Benzyl-2-oxazolidinone 99% (R)-4-Benzyl-2-oxazolidinone, 99%, ee:>99% (R)-4-Benzyl-2-oxazolidinone, >99% ee (R)-4-Benzyl-2-oxazolidinone,99%,>99% ee (R)-4-Benzyl-2-0xazolidinone (R)-(+)-4-Benzyl-2-xazolidineone (R)-4-Benzyl-2-oxazo (R)-4-Benzyl-2-oxazolidinone,99% (4R)-4-Benzyl-2-oxo-1,3-oxazolidine 2-OXAZOLIDINONE, 4-(PHENYLMETHYL)-, (4R)- 2-OXAZOLIDINONE, 4-PHENYL-, (4R)- (4R)-4-BENZYL-1,3-OXAZOLIDIN-2-ONE (4R)-4-BENZYLOXAZOLIDIN-2-ONE (4R)-4-PHENYL-1,3-OXAZOLIDIN-2-ONE (4R)-4-PHENYLOXAZOLIDIN-2-ONE 4-R-BENZYL-2-OXAZOLIDINONE (4R)-PHENYL-2-OXAZOLIDINONE (R)-PH-OXAZOLIDINONE (R)-4-BENZYL-OXAZOLIDIN-2-ONE (R)-(+)-4-BENZYL-2-OXAZOLIDINONE (R)-4-BENZYL-2-OXAZOLIDINONE (R)-(+)-4-BENZYL-2-OXAZOLIDONE (R)-(+)-4-Benzyl-2-oxazolidinone (R)-4-BenzyL (R)-4-Benzyl-2-oxazolidinone > -2-oxazoL (R)-4-Benzyl-2-oxazolidinone USP/EP/BP 4-benzyl-2-0xazolidinone (4R)-Phenylmethyl-2-oxazolidinone RBOX (R)-4-(PHENYLMETHYL)-2-OXAZOLIDINONE (R)-4-Benzyl-2-oxazolidinone CAS No. 102029-44-7 MLS00 OJOFMLDBXPDXLQ-SECBINFHSA-N TL806371 TB-2044 (R)-Solriamfetol Impurity 5 102029-44-7 102021-44-7 99319-52-1 102090-44-7 1022029-44-7 101029-44-7 Chiral Building Blocks Asymmetric Synthesis Glycidyl Compounds, etc. (Chiral) Chiral Auxiliaries Oxazolidinone Derivatives Asymmetric Synthesis