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Benzaldehyde, 2,4-bis[(2-methoxyethoxy)methoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 141330-16-7 Structure
  • Basic information

    1. Product Name: Benzaldehyde, 2,4-bis[(2-methoxyethoxy)methoxy]-
    2. Synonyms:
    3. CAS NO:141330-16-7
    4. Molecular Formula: C15H22O7
    5. Molecular Weight: 314.335
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 141330-16-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Benzaldehyde, 2,4-bis[(2-methoxyethoxy)methoxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzaldehyde, 2,4-bis[(2-methoxyethoxy)methoxy]-(141330-16-7)
    11. EPA Substance Registry System: Benzaldehyde, 2,4-bis[(2-methoxyethoxy)methoxy]-(141330-16-7)
  • 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: 141330-16-7(Hazardous Substances Data)

141330-16-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141330-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,3 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 141330-16:
(8*1)+(7*4)+(6*1)+(5*3)+(4*3)+(3*0)+(2*1)+(1*6)=77
77 % 10 = 7
So 141330-16-7 is a valid CAS Registry Number.

141330-16-7Relevant articles and documents

A thermally-stable enzyme detection assay that amplifies signal autonomously in water without assistance from biological reagents

Yeung, Kimy,Schmid, Kyle M.,Phillips, Scott T.

supporting information, p. 394 - 396 (2013/02/22)

This Communication describes a thermally-stable small molecule and a corresponding assay strategy that autonomously amplifies a colorimetric signal when a specific enzyme biomarker is detected. This journal is

BREAST CANCER RESISTANCE PROTEIN (BCRP) INHIBITOR

-

Page/Page column 14, (2010/02/14)

The invention provides a drug which inhibits BCRP. A breast cancer resistance protein inhibitor containing, as an active ingredient, a diphenylacrylonitrile derivative represented by the following formula (1): [wherein, each of 8 R's, which are the same or different from one another, represents a hydrogen atom, a hydroxyl group, a nitro group, an amino group, an acetylamino group (-NHCOCH3 group), a cyano group (-CN group), a formyl group (-CHO group), -COOR1 (R1 is hydrogen or C1-C4 alkyl) , -O(CH2)nCOOR2 (n=1-7: R2 is hydrogen or C1-C4 alkyl) , -OOCCH2CH2COOR3 (R3 is hydrogen, C1-C4 alkyl, (Z)-2-(3,4-dimethoxy-phenyl)-3-(4-hydroxy-phenyl)-acrylonitrile, or glycopyranosyl), a C1-C8 alkoxy group, a C1-C4 alkyl group, a halogen atom, a C1-C4 alkoxy C1-C4 alkoxy C1-C4 alkoxy group, a C2-C8 acyloxy group, a C2-C8 halogenoacyloxy group, a methylenedioxy group, a trifluoromethyl group, a phosphate group (i.e., -OP(O) (OH)2) or a salt thereof, a sulfate group (i.e., -OSO3H) or a salt thereof, a glycopyranosyl group or a salt thereof, a phosphate ester of a glycopyranosyl group or a salt of the ester, a sulfate ester of a glycopyranosyl group or a salt of the ester, or a piperidinopiperidinocarbonyloxy group], an ester thereof, or a salt thereof.

Enantioselective acylation of 2-hydroxymethyl-2,3-dihydrobenzofurans catalysed by lipase from Pseudomonas cepacia (Amano PS) and total stereoselective synthesis of (-)-(R)-MEM-protected arthrographol

Ramadas,Krupadanam, G. L. David

, p. 3375 - 3393 (2007/10/03)

Lipase Amano PS catalysed acylation of (±)-2-hydroxymethyl-2,3-dihydrobenzofurans using vinyl acetate as the acyl donor in n-hexane gave (-)-(R)-2-acetoxymethyl-2,3-dihydrobenzofurans and (+)-(S)-2-hydroxymethyl-2,3-dihydrobenzofurans in high enantiomeric excess. (-)-(R)-Acetate 18j is converted to (-)-(R)-MEM-protected arthrographol 22. Copyright (C) 2000 Elsevier Science Ltd.

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