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227471-72-9

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227471-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 227471-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,7,4,7 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 227471-72:
(8*2)+(7*2)+(6*7)+(5*4)+(4*7)+(3*1)+(2*7)+(1*2)=139
139 % 10 = 9
So 227471-72-9 is a valid CAS Registry Number.

227471-72-9SDS

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 (3,3-diphenylbenzo[f]chromen-5-yl)methanol

1.2 Other means of identification

Product number -
Other names 3,3-diphenyl-5-hydroxymethyl-<3H>-naphtho-<2,1-b>-pyrane

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:227471-72-9 SDS

227471-72-9Relevant articles and documents

Synthesis and complexation properties of photochromic benzochromenes containing aza- and diaza- 18-crown-6-ether fragments

Fedorova,Strokach,Chebun'kova,Valova,Gromov,Alfimov,Lokshin,Samat

, p. 287 - 294 (2006)

Complex formation of Mg2+, Ba2+, and Pb2+ perchlorates with 3,3-diphenyl-3H-benzo[f]chromenes containing aza-and diaza-18-crown-6-ether or morpholine fragments was studied. The strong influence of the metal cations on the

Photochromic spin traps. Part IV. ? 3,3-Diphenyl-5-[2-(N-tert-butylethanalnitrone)]-[3H]-naphtho[2,1-b]pyran

Alberti, Angelo,Campredon, Mylene,Giusti, Gerard,Luccioni-Houze, Barbara,Macciantelli, Dante

, p. 775 - 781 (2007/10/03)

The title compound, a nitrone of the chromene series exhibiting photochromic properties, was synthesized and ESR studies proved its ability to act as a spin trapping agent. Although in general the aminoxyls formed in the trapping process did not exhibit any evidence of opening of the heterocyclic ring, both the closed and open forms have been observed for the spin adduct of the methyl radical. The rate constant for ring closure, i.e. the conversion of the latter isomer into the former upon ceasing optical excitation, was measured as 7 × 10-3-1 s at 20°C. The new photochromic nitrone did not exhibit a significant stabilizing effect towards Corn Yellow, a typical photochromic compound, but its action was synergistic to that of popular commercial additives. Copyright

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