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98243-83-5

Benalaxyl-M is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 98243-83-5 Structure

  • Basic information

    1. Product Name: Benalaxyl-M
    2. Synonyms: Benalaxyl-M;N-(2,6-Dimethylphenyl)-N-(phenylacetyl)-D-alanine methyl ester;Benalaxyl-m [iso];D-Alanine, N-(2,6-diMethylphenyl)-N-(phenylacetyl)-, Methyl ester;(R)-Methyl 2-(N-(2,6-diMethylphenyl)-2-phenylacetaMido)propanoate;(R)-Benalaxyl;(S)-methyl 2-(N-(2,6-dimethylphenyl)-2-phenylacetamido)pro
    3. CAS NO:98243-83-5
    4. Molecular Formula: C20H23NO3
    5. Molecular Weight: 325.4
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 98243-83-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 468.8°Cat760mmHg
    3. Flash Point: 237.3°C
    4. Appearance: /
    5. Density: 1.131g/cm3
    6. Vapor Pressure: 5.8E-09mmHg at 25°C
    7. Refractive Index: 1.574
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. CAS DataBase Reference: Benalaxyl-M(CAS DataBase Reference)
    11. NIST Chemistry Reference: Benalaxyl-M(98243-83-5)
    12. EPA Substance Registry System: Benalaxyl-M(98243-83-5)

  • Safety Data

    1. Hazard Codes: N
    2. Statements: 51/53
    3. Safety Statements: 61
    4. RIDADR: UN3077 9/PG 3
    5. WGK Germany: 2
    6. RTECS:
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 98243-83-5(Hazardous Substances Data)

98243-83-5 Usage

Uses

(R)-Benalaxyl is the R-enantiomer of Benalaxyl (B131900) an acylamino acid fungicide.

Definition

ChEBI: A methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate that is the more active R-enantiomer of benalaxyl.

Check Digit Verification of cas no

The CAS Registry Mumber 98243-83-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,2,4 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 98243-83:
(7*9)+(6*8)+(5*2)+(4*4)+(3*3)+(2*8)+(1*3)=165
165 % 10 = 5
So 98243-83-5 is a valid CAS Registry Number.
InChI:InChI=1/C20H23NO3/c1-14-9-8-10-15(2)19(14)21(16(3)20(23)24-4)18(22)13-17-11-6-5-7-12-17/h5-12,16H,13H2,1-4H3/t16-/m1/s1

98243-83-5SDS

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 benalaxyl-M

1.2 Other means of identification

Product number -
Other names kiralaxyl

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:98243-83-5 SDS

98243-83-5Upstream product

98243-83-5Downstream Products

98243-83-5Relevant articles and documents

Stereoselective metabolism of benalaxyl in liver microsomes from rat and rabbit

Zhang, Ping,Zhu, Wentao,Dang, Ziheng,Shen, Zhigang,Xu, Xinyuan,Huang, Ledan,Zhou, Zhiqiang

, p. 93 - 98 (2011)

Benalaxyl (BX), methyl-N-phenylacetyl-N-2,6-xylyl alaninate, is a potent acylanilide fungicide and consist of a pair of enantiomers. The stereoselective metabolism of BX was investigated in rat and rabbit microsomes in vitro. The degradation kinetics and

Chiral separation of basic compounds on sulfated β-cyclodextrin-coated zirconia monolith by capillary electrochromatography

Hong, Jong-Seong,Park, Jung Hag

, p. 1809 - 1813 (2013/07/26)

Sulfated β-cyclodextrin (SCD)-coated zirconia monolith was used as the chiral stationary phase in capillary electrochromatography for enantiomeric separation of basic chiral compounds. SCD adsorbed on the zirconia surface provided a stable chiral stationary phase in reversed-phase eluents. Retention, chiral selectivity and resolution of a set of six basic chiral compounds were measured in eluents of varying pH, composition of methanol and buffer. Optimum mobile phase condition for the separation of the compounds was found to be methanol content of 30%, buffer concentration of 30 mM and pH of 4.0.

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