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125161-79-7

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125161-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125161-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,6 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 125161-79:
(8*1)+(7*2)+(6*5)+(5*1)+(4*6)+(3*1)+(2*7)+(1*9)=107
107 % 10 = 7
So 125161-79-7 is a valid CAS Registry Number.

125161-79-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-bromo-3-methylpentyl) acetate

1.2 Other means of identification

Product number -
Other names 5-Bromo-3-methylpentyl acetate

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:125161-79-7 SDS

125161-79-7Relevant articles and documents

PHEROMONES OF INSECTS AND THEIR ANALOGS. XX. METHYL-BRANCHED PHEROMONES BASED ON 4-METHYLTETRAHYDROPYRAN. I. SYNTHESIS OF RACEMIC 4,8-DIMETHYLDECANAL - THE PHEROMONE OF THE FLOUR BEETLES Tribolium confusum AND Tribolium castaneum

Odinokov, V. N.,Izhmuratov, G. Yu.,Kharisov, R. Ya.,Ibragimov, A. G.,Sultanov, R. M.,et al.

, p. 236 - 239 (2007/10/02)

A synthesis is proposed of 4,8-dimethyldecanal (VIII) - a pheromone of the flour beetles Tribolium confusum and T. castaneum.By heating 71.2 g of 4-methyltetrahydropyran (I), 83.2 g of AcBr and 1.57 g ZnCl2 (45 deg C , then 120 deg C, 2h), 1-acetoxy-5-bromo-3-methylpentane (II) was obtained.The hydrolysis of 19.8 g of (II) ( MeOH-H2O, TsOH, 20 deg C, 15h) gave 5-bromo-3-methylpentan-1-ol (III).From 18.1 g of (III) and 38.9 ml of 2,3-dihydropyran (Et2O, TsOH, 20 deg C, 20h) was obtained the 2-THPL ester of (III), (IV), which was converted into 3-methyloct-7-en-1-ol (V) by the treatment of the corresponding Grignard reagent with allyl bromide (THF, CuI-bi-2-pyridyl, 2 deg C, 4 h, Ar).The interaction of 1.42 g of (V) with Et3Al (hexane, 20 deg C, Cp2ZrCl2, Ar) gave 3,7-dimethylnonan-1-ol (VI), boiling which with 48percent HBr in the presence of concentrated H2SO4 gave 1-bromo-3,7-dimethylnonane (VII) which was then converted into the desired (VIII) by the reaction of the corresponding Grignard reagent with DMFA ( 0-2 deg C, 1 h; 20 deg C, 2h; Ar).The characteristics of the compounds - yield (percent), nD (deg C): (I), 79, 1.4340 (22); (III) 89, 1.4660 (23); (IV), 82, 1.4739 (23); (V), 85, -; (VI) , 90, 1.4483 (20); (VII), 88, 1.4409 (22); (VIII), 88, 1.4589 (22).Details of the IR and PMR spectra of the compounds (II) - (VII) are given.

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