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761460-03-1

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761460-03-1 Usage

General Description

(R)-4-Boc-3-morpholineacetic acid is a chemical compound that is used in the synthesis of pharmaceuticals and as an intermediate in organic chemistry. It is a derivative of morpholine and contains a Boc (tert-butoxycarbonyl) protecting group, making it suitable for use in peptide synthesis. (R)-4-Boc-3-morpholineacetic acid has potential applications in the development of drugs and is also used as a building block for the creation of complex molecules. Its specific properties and reactivity make it a valuable tool for chemical synthesis and drug discovery research.

Check Digit Verification of cas no

The CAS Registry Mumber 761460-03-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,1,4,6 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 761460-03:
(8*7)+(7*6)+(6*1)+(5*4)+(4*6)+(3*0)+(2*0)+(1*3)=151
151 % 10 = 1
So 761460-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H19NO5/c1-11(2,3)17-10(15)12-4-5-16-7-8(12)6-9(13)14/h8H,4-7H2,1-3H3,(H,13,14)/t8-/m1/s1

761460-03-1 Well-known Company Product Price

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  • Aldrich

  • (669830)  (R)-4-Boc-3-morpholineaceticacid  ≥97.5% (HPLC)

  • 761460-03-1

  • 669830-250MG

  • 2,640.69CNY

  • Detail
  • Aldrich

  • (669830)  (R)-4-Boc-3-morpholineaceticacid  ≥97.5% (HPLC)

  • 761460-03-1

  • 669830-1G

  • 8,628.75CNY

  • Detail

761460-03-1SDS

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 2-[(3R)-4-[(2-methylpropan-2-yl)oxycarbonyl]morpholin-3-yl]acetic acid

1.2 Other means of identification

Product number -
Other names (R)-3-CARBOXYMETHYL-MORPHOLINE-4-CARBOXYLIC ACID TERT-BUTYL ESTER

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:761460-03-1 SDS

761460-03-1Relevant articles and documents

SUBSTITUTED MORPHOLINES AS MODULATORS FOR THE CALCIUM SENSING RECEPTOR

-

, (2014/02/15)

Compounds of Formula (I) along with processes for their preparation that are useful for treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (CaSR) receptors. Methods of treating, managing and/or lessening the diseases, disorders, syndromes or conditions associated with the modulation of calcium sensing (CaSR) receptors of Formula (I).

Process for producing enantiopure beta-amino acid derivatives, and enantiopure beta-amino acid derivatives

-

, (2008/06/13)

Process for producing enantiopure β-amino acid derivatives corresponding to general formula (I) R1-NZ-CHR2—CH2—COOR3 (I) in which R1 and R2 independently denote organic residues optionally forming a cyclic substituent, R3 denotes H or an organic residue, and Z represents H or an amino function-protecting group, comprising a step in which a mixture of enantiomers of a compound corresponding to general formula (II) R1-NZ-CHR2—CH2—COOR4 (II) in which R1, R2 and Z are as defined for formula (I), and R4 is an organic residue, is subjected to hydrolysis in the presence of a lipase.

Enzymatic resolution of cyclic N-Boc protected β-aminoacids

Pousset, Cyrille,Callens, Roland,Haddad, Mansour,Larcheveque, Marc

, p. 3407 - 3412 (2007/10/03)

Methyl and ethyl esters of N-Boc homoproline, homopipecolic acid and 3-carboxymethyl-morpholine were kinetically resolved by hydrolysis catalysed by Burkholderia cepacia lipase to give the corresponding acids and residual esters in enantiomeric excesses better than 99% (E > 100).

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