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Butanedioic acid, methyl-, 1-(phenylmethyl) ester, (2R)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143225-28-9 Structure
  • Basic information

    1. Product Name: Butanedioic acid, methyl-, 1-(phenylmethyl) ester, (2R)- (9CI)
    2. Synonyms: Butanedioic acid, methyl-, 1-(phenylmethyl) ester, (2R)- (9CI);(2R)-Methylbutanedioic acid 1-(phenylmethyl) ester;(R)-Methylbutanedioic acid 1-(phenylmethyl) ester
    3. CAS NO:143225-28-9
    4. Molecular Formula: C12H14O4
    5. Molecular Weight: 222.23716
    6. EINECS: N/A
    7. Product Categories: ACIDHALIDE
    8. Mol File: 143225-28-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.189
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Butanedioic acid, methyl-, 1-(phenylmethyl) ester, (2R)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: Butanedioic acid, methyl-, 1-(phenylmethyl) ester, (2R)- (9CI)(143225-28-9)
    11. EPA Substance Registry System: Butanedioic acid, methyl-, 1-(phenylmethyl) ester, (2R)- (9CI)(143225-28-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 143225-28-9(Hazardous Substances Data)

143225-28-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 143225-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,2 and 5 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143225-28:
(8*1)+(7*4)+(6*3)+(5*2)+(4*2)+(3*5)+(2*2)+(1*8)=99
99 % 10 = 9
So 143225-28-9 is a valid CAS Registry Number.

143225-28-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-4-(Benzyloxy)-3-methyl-4-oxobutanoic acid

1.2 Other means of identification

Product number -
Other names MESYLOXY-1-(N-(((4-NITROBENZYL)OXY)CARBONYL)ACETOIMIDOYL)PYRROLIDINE

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:143225-28-9 SDS

143225-28-9Downstream Products

143225-28-9Relevant articles and documents

Sensing remote chirality: Stereochemical determination of β-, γ-, and δ-chiral carboxylic acids

Tanasova, Marina,Anyika, Mercy,Borhan, Babak

supporting information, p. 4274 - 4278 (2015/04/14)

Determining the absolute stereochemisty of small molecules bearing remote nonfunctionalizable stereocenters is a challenging task. Presented is a solution in which appropriately substituted bis(porphyrin) tweezers are used. Complexation of a suitably derivatized β-, γ-, or δ-chiral carboxylic acid to the tweezer induces a predictable helicity of the bis(porphyrin), which is detected as a bisignate Cotton Effect (ECCD). The sign of the ECCD curve is correlated with the absolute stereochemistry of the substrate based on the derived working mnemonics in a predictable manner.

Retroviral protease inhibitors

-

, (2008/06/13)

N-heterocyclic moiety-containing hydroxyethylamine protease inhibitor compounds, methods for making the compounds, and intermediates useful in the method. Also, a method for inhibiting retroviral proteases and for treatment or prophylaxis of a retroviral infection.

RETROVIRAL PROTEASE INHIBITORS

-

, (2008/06/13)

N-heterocyclic moiety containing hydroxyethylamine compounds are effective as retroviral protease inhibitors, and in particular as inhibitors of HIV protease.

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