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1-chloro-2-methylheptane is an organic compound with the molecular formula C8H17Cl. It is a colorless liquid at room temperature and has a chlorinated alkane structure. The compound consists of a heptane chain with a methyl group attached to the second carbon and a chlorine atom attached to the first carbon. 1-chloro-2-methylheptane is used as a solvent, a chemical intermediate, and in the synthesis of various pharmaceuticals and agrochemicals. It is also known for its potential use as a gasoline additive and as a component in the production of lubricants. Due to its chemical properties, it is important to handle 1-chloro-2-methylheptane with care, as it can be harmful if inhaled or absorbed through the skin.

2350-16-5

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2350-16-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2350-16-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2350-16:
(6*2)+(5*3)+(4*5)+(3*0)+(2*1)+(1*6)=55
55 % 10 = 5
So 2350-16-5 is a valid CAS Registry Number.

2350-16-5Upstream product

2350-16-5Downstream Products

2350-16-5Relevant academic research and scientific papers

Do enzymes recognise remotely located stereocentres? Highly enantioselective Candida rugosa lipase-catalysed esterification of the 2- to 8-methyldecanoic acids

Hedenstroem, Erik,Nguyen, Ba-Vu,Silks III, Louis A.

, p. 835 - 844 (2007/10/03)

Several racemic methyl decanoic acids have been synthesised and successfully resolved in esterification with 1-hexadecanol at aw=0.8 in cyclohexane using immobilised Candida rugosa lipase (CRL) as the catalyst. The enantiomeric ratios (E=2.8-68) obtained were surprisingly high even when the methyl group was as remotely located as in 8-methyldecanoic acid (E=25). Interestingly, the lipase shows enantiopreference for the S-enantiomer when the methyl group is located on even numbered carbons i.e. for the 2-,4-,6- and 8-methyldecanoic acids and to the R-enantiomer when the methyl group is located on uneven numbered carbons i.e. for the 3-,5- and 7-methyldecanoic acids.

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