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  • 1454653-03-2 Structure
  • Basic information

    1. Product Name: C15H22O3
    2. Synonyms:
    3. CAS NO:1454653-03-2
    4. Molecular Formula:
    5. Molecular Weight: 250.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1454653-03-2.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: C15H22O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C15H22O3(1454653-03-2)
    11. EPA Substance Registry System: C15H22O3(1454653-03-2)
  • 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: 1454653-03-2(Hazardous Substances Data)

1454653-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1454653-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,4,6,5 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1454653-03:
(9*1)+(8*4)+(7*5)+(6*4)+(5*6)+(4*5)+(3*3)+(2*0)+(1*3)=162
162 % 10 = 2
So 1454653-03-2 is a valid CAS Registry Number.

1454653-03-2Upstream product

1454653-03-2Downstream Products

1454653-03-2Relevant articles and documents

Structural optimization of super-gelators derived from naturally-occurring mannose and their morphological diversity

Ono, Fumiyasu,Watanabe, Hisayuki,Shinkai, Seiji

, p. 25940 - 25947 (2014)

Mannose derivatives were synthesized as low molecular-weight gelators with various alkoxy substituents on the aromatic ring of methyl-4,6-O-benzilidene- α-d-mannopyranoside. Most of these mannose derivatives could gel in various solvents, such as octane, cyclohexane, toluene, ethylene glycol and ethanol solutions, at concentrations lower than 2.0 wt%. In particular, the critical gelation concentration (CGC) of methyl-4,6-O-(4-butoxybenzylidene)- α-d-mannopyranoside (2) for squalane was only 0.025 wt%, one of the lowest CGCs we have ever experienced. The observations of xerogels by FE-SEM, TEM and AFM revealed that the length of the alkoxy chains of the mannose derivatives influences the gel morphologies. Moreover, the toluene gels formed from the mannose derivatives 1-6 functionalized by a linear alkoxy group exhibited thixotropic properties. Interestingly, the gels of various solvents formed from methyl-4,6-O-(4-dodecyloxybenzylidene)-α-d-mannopyranoside (6) (with the longest alkoxy chain on the aromatic ring in this paper) exhibited thixotropic properties. Thus, we confirmed that alkoxy groups on the aromatic ring exert noticeable effects on the gelation properties of these mannose derivatives. the Partner Organisations 2014.

NOVEL SUGAR-DERIVED GELATOR

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Paragraph 0144; 0145; 0146; 0148; 0159, (2015/02/18)

There is provided a novel gelator containing a sugar derivative. A gelator including a compound of Formula (1) or Formula (2): wherein each of R1 and R3 is independently a linear or branched alkyl group having a carbon atom number of 1 to 20, a cyclic C3-20 alkyl group, or a linear or branched alkenyl group having a carbon atom number of 2 to 20, n is 0 or an integer of 1 to 4, R2 is a hydrogen atom, a linear or branched alkyl group having a carbon atom number of 1 to 10, or an aryl group optionally having a substituent, and R4 and R5 are each a hydroxy group.

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