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(R)-(+)-4-(Hydroxymethyl)-2-oxazolidinone benzoate is a white to off-white crystalline powder that is soluble in polar solvents such as methanol and ethanol. It is a chemical compound commonly used as an intermediate in organic synthesis and has a unique chemical structure and reactivity.
Used in Pharmaceutical Research and Development:
(R)-(+)-4-(Hydroxymethyl)-2-oxazolidinone benzoate is used as a building block for the synthesis of various drugs and pharmaceutical products. Its unique chemical structure and reactivity make it a valuable component in the development of new medications.
Used in Agrochemicals:
(R)-(+)-4-(Hydroxymethyl)-2-oxazolidinone benzoate is used as an intermediate in the synthesis of agrochemicals. Its unique properties allow it to be incorporated into the development of new and effective products for agricultural applications.
Used in Fine Chemicals:
(R)-(+)-4-(Hydroxymethyl)-2-oxazolidinone benzoate is also used in the field of fine chemicals due to its unique chemical structure and reactivity. This allows it to be utilized in the creation of specialty chemicals for various industries.

136015-44-6

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136015-44-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136015-44-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,0,1 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 136015-44:
(8*1)+(7*3)+(6*6)+(5*0)+(4*1)+(3*5)+(2*4)+(1*4)=96
96 % 10 = 6
So 136015-44-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO4/c13-10(8-4-2-1-3-5-8)15-6-9-7-16-11(14)12-9/h1-5,9H,6-7H2,(H,12,14)/t9-/m1/s1

136015-44-6 Well-known Company Product Price

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  • Aldrich

  • (515558)  (R)-(+)-4-(Hydroxymethyl)-2-oxazolidinonebenzoate  97%

  • 136015-44-6

  • 515558-1G

  • 2,817.36CNY

  • Detail

136015-44-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [(4R)-2-Oxo-1,3-oxazolidin-4-yl]methyl benzoate

1.2 Other means of identification

Product number -
Other names 1,4-dithiaspiro[4.5]dec-8-yl benzoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:136015-44-6 SDS

136015-44-6Relevant academic research and scientific papers

Synthesis and Inhibitory Mechanisms of Phospholipase A2 Inhibitors

Katsumura,Iwama,Inagaki,Fujii,Ikeda

, p. 225 - 229 (2007/10/03)

Two types of Phospholipase A2 (PLA2) inhibitor were synthesized, one of which was a terpenoid having unsaturated aldehyde, and the other was a cyclic phospholipid analog. The inhibitory mechanisms of each compound were proposed. Thus, the former may irreversibly modify an interfacial recognition site, and the latter competitively binds to the catalytic site of PLA2 with the mode similar to that of the genuine substrate.

A new route for protected amino alcohols from (R)-glycidol. Copper(I) mediated alkylation of 4-tosyloxymethyl-2-oxazolidinone

Iwama,Katsumura

, p. 3363 - 3365 (2007/10/02)

The reaction of (S)-4-tosyloxymethyl-2-oxazolidinone, which was synthesized from (R)-glycidol through (R)-4-benzoyloxymethyl-2-oxazolidinone, with various lithium dialkylcuprate(I)s in THF proceeded smoothly to afford the corresponding protected amino alcohol derivatives in good yield.

Synthesis of Optically Pure 4-Hydroxymethyloxazolidinone as Chiral Serinol Synthon from Glycidol

Katsumura, Shigeo,Kondo, Akihiro,Han, Quingjun

, p. 1245 - 1248 (2007/10/02)

Optically pure 3-benzyl-4-hydroxymethyl-2-oxazolidinone and 4-benzoyloxymethyl-2-oxazolidinone as chiral serinol synthons were synthesized from optically active glycidol by intramolecular cyclization via 2,3-epoxycarbamates with strict SN2 beha

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