RE: ORGLIST: Re: Everybody Digest, Vol 12, Issue 5

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From: Maringanti Krishna (maringanti9$##$yahoo.com)
Date: Tue Sep 13 2005 - 11:51:43 EDT


Richard:
What is the half life of benzyl chloride in water at
-4 deg. c.??
Many thanks
Krishna

--- Richard Prankerd
<Richard.Prankerd$##$vcp.monash.edu.au> wrote:

> Pathi:
>
> "Stable" is a relative term. If you leave benzyl
> chloride exposed to water at RT, or even in a
> refrigerator for long enough, the benzyl chloride
> will eventually hydrolyse to benzyl alcohol.
>
> Nothing is really "stable"
>
> Richard
>
> Richard J. Prankerd, PhD
> Senior Lecturer
> Victorian College of Pharmacy, Monash University
> 381 Royal Pde., Parkville VIC 3052
>
> Phone: INT+613-9903-9003
> Phax: INT+613-9903-9583
>
> Drugs need to be designed with delivery components
> in mind - Takeru Higuchi
>
>
> > -----Original Message-----
> > From: everybody-bounces$##$orglist.net
> > [mailto:everybody-bounces$##$orglist.net] On Behalf
> Of
> > Lakshmipathi Pandarinathan
> > Sent: Sunday, 11 September 2005 3:55 AM
> > To: everybody$##$orglist.net
> > Subject: ORGLIST: Re: Everybody Digest, Vol 12,
> Issue 5
> >
> >
> > M.Patel
> > Benzyl chloride can be converted to benzyl alcohol
> by heating benzyl
> > chloride in water at 50-60 deg C for 2 hrs. But at
> room
> > temperature benzyl
> > chloride is stable in water.
> > Pathi
> >
> > ----- Original Message -----
> > From: <everybody-request$##$orglist.net>
> > To: <everybody$##$orglist.net>
> > Sent: Saturday, September 10, 2005 12:02 PM
> > Subject: Everybody Digest, Vol 12, Issue 5
> >
> >
> > > Send Everybody mailing list submissions to
> everybody$##$orglist.net
> > >
> > > To subscribe or unsubscribe via the World Wide
> Web, visit
> > >
> http://two.pairlist.net/mailman/listinfo/everybody
> > > or, via email, send a message with subject or
> body 'help' to
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> > >
> > > When replying, please edit your Subject line so
> it is more specific
> > > than "Re: Contents of Everybody digest..."
> > >
> > >
> > > Today's Topics:
> > >
> > > 1. guidance (starscientific)
> > > 2. NABH4 reductive power enhancement
> (diogo$##$unilavras.edu.br)
> > > 3. p-Cresol to 4-MCH (Kamal)
> > > 4. aminohydroxynaphtoic acids (Gianluca
> Sbardella)
> > > 5. Process of PGR-PACLOBUTRAZOLE or
> Lab.scale technology.
> > > (Chhaganbhai Madhubhai)
> > >
> > >
> > >
> >
>
----------------------------------------------------------------------
> > >
> > > Message: 1
> > > Date: Thu, 8 Sep 2005 10:08:10 +0530
> > > From: "starscientific"
> <info$##$starscientificindia.com>
> > > Subject: ORGLIST: guidance
> > > To: <everybody$##$orglist.net>
> > > Message-ID:
> <000c01c5b470$a9edd4c0$d40110ac$##$hatway.net>
> > > Content-Type: text/plain; charset="iso-8859-1"
> > >
> > > Hi Everybody,
> > >
> > > Can Benzyl Chloride react with water, and which
> under conditions?
> > > please
> > > inform me
> > >
> > > Thanks in Advance
> > > M.Patel
> > > -------------- next part --------------
> > > An HTML attachment was scrubbed...
> > > URL:
> > >
> >
>
http://two.pairlist.net/pipermail/everybody/attachments/200509
> > 08/3f6ce042/attachment-0001.html
> > >
> > > ------------------------------
> > >
> > > Message: 2
> > > Date: Thu, 8 Sep 2005 22:42:46 -0300 (BRT)
> > > From: diogo$##$unilavras.edu.br
> > > Subject: ORGLIST: NABH4 reductive power
> enhancement
> > > To: everybody$##$orglist.net
> > > Message-ID:
> > >
>
<61439.200.159.218.226.1126230166.squirrel$##$webmail.unilavras.edu.br>
> > > Content-Type: text/plain;charset=iso-8859-1
> > >
> > > Hello everybody...
> > > Ive been reading some papers from the 70's thar
> discuss on
> > the ways
> > > of enhancing NABH4 power of reduction, as with
> CoCl2 and
> > I2. Do any of
> > > you have some references that discuss it in more
> details,
> > mainly about
> > > the selectivities in this reactions over
> different
> > reducible groups?
> > > Thanks, Diogo
> > >
> > >
> > > ------------------------------
> > >
> > > Message: 3
> > > Date: Fri, 9 Sep 2005 18:54:09 +0530
> > > From: "Kamal" <mailbox$##$invalid>
> > > Subject: ORGLIST: p-Cresol to 4-MCH
> > > To: <everybody$##$orglist.net>
> > > Message-ID:
> <001401c5b541$c2c52990$cc6afea9$##$kamal>
> > > Content-Type: text/plain; charset="iso-8859-1"
> > >
> > > Hi to all !
> > >
> > > I'm looking for some old references (1927-28)
> suggesting one-step
> > > synthesis of p-Cresol to 4-Methyl Cyclohexanone.
> > >
> > > Can anyone pls suggest me this or such same
> references ?
> > >
> > > Awaiting yr suggetions !
> > >
> > >
> > >
> > >
> > > Best wishes, from,
> > > Kamal
> > > -------------- next part --------------
> > > An HTML attachment was scrubbed...
> > > URL:
> > >
> >
>
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> > 09/7b517100/attachment-0001.html
> > >
> > > ------------------------------
> > >
> > > Message: 4
> > > Date: Fri, 9 Sep 2005 18:22:10 +0200
> > > From: "Gianluca Sbardella" <gsbardella$##$unisa.it>
> > > Subject: ORGLIST: aminohydroxynaphtoic acids
> > > To: <everybody$##$orglist.net>
> > > Message-ID:
> <005001c5b55a$aa312a00$c5a5cdc1$##$GSMerlino>
> > > Content-Type: text/plain; charset="us-ascii"
> > >
> > > Dear colleagues,
> > >
> > > I was looking for references concerning the
> preparation of
> > > 2-amino-5-hydroxy-7-naphthoic acid and actually
> I found the
> > following:
> > >
> > > Hopper, I. V.; Syme, A. C.; Wilson, F. J.
> > Aminohydroxynaphthoic acids.
> > > Journal of the Society of Dyers and Colourists
> (1942), 58 93-7
> > >
>
=== message truncated ===



                
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