Welcome to LookChem.com Sign In|Join Free

CAS

  • or

27000-00-6

Post Buying Request

27000-00-6 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

27000-00-6 Usage

General Description

METHYL (R)-2-HYDROXY-3-PHENYLPROPIONATE is a chemical compound with the molecular formula C11H14O3. It is a methyl ester of (R)-2-hydroxy-3-phenylpropionic acid, a chiral compound that is commonly used in the synthesis of pharmaceuticals and organic compounds. This chemical is often used as a chiral auxiliary in asymmetric synthesis to introduce chirality into molecules. It is also utilized in the production of fragrances and flavors due to its pleasant aroma and taste. Additionally, METHYL (R)-2-HYDROXY-3-PHENYLPROPIONATE has potential applications in the development of new drugs and biologically active compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 27000-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,0 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27000-00:
(7*2)+(6*7)+(5*0)+(4*0)+(3*0)+(2*0)+(1*0)=56
56 % 10 = 6
So 27000-00-6 is a valid CAS Registry Number.

27000-00-6 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (M2350)  Methyl D-3-Phenyllactate  >98.0%(GC)

  • 27000-00-6

  • 1g

  • 590.00CNY

  • Detail
  • TCI America

  • (M2350)  Methyl D-3-Phenyllactate  >98.0%(GC)

  • 27000-00-6

  • 5g

  • 1,850.00CNY

  • Detail

27000-00-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl (2R)-2-hydroxy-3-phenylpropanoate

1.2 Other means of identification

Product number -
Other names (R)-2-Hydroxy-3-phenylpropionic Acid Methyl 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:27000-00-6 SDS

27000-00-6Relevant articles and documents

Butane-2,3-diacetal-desymmetrized glycolic acid - A new building block for the stereoselective synthesis of enantiopure α-hydroxy acids

Diez, Elena,Dixon, Darren J.,Ley, Steven V.

, p. 2906 - 2909 (2001)

According to a chiral memory protocol, a chiral glycolic acid equivalent, the butane-2,3-diacetal-desymmetrized glycolate 2, is obtained from chiral 3-halopropane-1,2-diols 1. Compound 2 is a new and effective building block for the synthesis of mono- and

Total Synthesis of (+)-Prunustatin A: Utility of Organotrifluoroborate-Mediated Prenylation and Shiina MNBA Esterification and Macrolactonization to Avoid a Competing Thorpe-Ingold Effect Accelerated Transesterification

Chojnacka, Maja W.,Batey, Robert A.

supporting information, p. 5671 - 5675 (2018/09/13)

A convergent total synthesis of (+)-prunustatin A is described through the assembly of two key fragments and a macrolactonization. Shiina MNBA couplings were used for the formation of each of the four ester bonds in the tetralactone ring, including the key macrocyclization which was essential to minimize competing Thorpe-Ingold accelerated transesterification. Other key steps included an organoboron-based prenylation using potassium prenyltrifluoroborate and a carbonyldiimidazole-mediated coupling to form the salicylamide.

Asymmetric Assembly of All-Carbon Tertiary/Quaternary Nonadjacent Stereocenters through Organocatalytic Conjugate Addition of α-Cyanoacetates to a Methacrylate Equivalent

Iriarte, Igor,Vera, Silvia,Badiola, Eider,Mielgo, Antonia,Oiarbide, Mikel,García, Jesús M.,Odriozola, José M.,Palomo, Claudio

, p. 13690 - 13696 (2016/09/13)

An efficient, highly diastereo- and enantioselective assembly of acyclic carbonyl fragments possessing nonadjacent all-carbon tertiary/quaternary stereoarrays is reported based on a Br?nsted base catalyzed Michael addition/α-protonation sequence involving α-cyanoacetates and 2,4-dimethyl-4-hydroxypenten-3-one as novel methacrylate equivalent.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 27000-00-6