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173852-01-2

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173852-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173852-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,8,5 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 173852-01:
(8*1)+(7*7)+(6*3)+(5*8)+(4*5)+(3*2)+(2*0)+(1*1)=142
142 % 10 = 2
So 173852-01-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H14O2/c1-3-4-5-11-6-8-12(9-7-11)14-10(2)13/h3,6-9H,1,4-5H2,2H3

173852-01-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-but-3-enylphenyl) acetate

1.2 Other means of identification

Product number -
Other names Acetyl-chavicol

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:173852-01-2 SDS

173852-01-2Relevant articles and documents

About the "physiological size" of fluorine substituents : Comparison of sensorially active compounds with fluorine and methyl substituted analogues

Schlosser, Manfred,Michel, Dominique

, p. 99 - 108 (1996)

The taste of four fluoro substituted derivatives (2a, 2b, 2c and 2d) is almost indistinguishable from that of the parent compound 4-(4-hydroxyphenyl)butan-2-one (1), the main flavor component of raspberries. The same holds for the comparison between the corresponding acetate, another raspberry ingredient, and its 1-fluoro analogue (2e). In contrast, methyl substituents (as present in compounds 3a, 3b, 3c, 3d and 3e) profoundly alter the organoleptic properties. - The preparation of the fluorinated derivatives (2) involved the three principal options existing for the incorporation of fluorine into organic molecular skeletons : the use of "prefabricates" (i.e., of fluoroaromatic building blocks), the formation of chlorofluorocarbene cycloadducts followed by their solvolytic ring opening and the addition of fluoride to olefinic double bonds. Copyright

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