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6607-66-5

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6607-66-5 Usage

Uses

1,3,3-Trimethoxybutane may be used in chemical synthesis studies.

Check Digit Verification of cas no

The CAS Registry Mumber 6607-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,0 and 7 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6607-66:
(6*6)+(5*6)+(4*0)+(3*7)+(2*6)+(1*6)=105
105 % 10 = 5
So 6607-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O3/c1-7(9-3,10-4)5-6-8-2/h5-6H2,1-4H3

6607-66-5 Well-known Company Product Price

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  • Aldrich

  • (197882)  1,3,3-Trimethoxybutane  97%

  • 6607-66-5

  • 197882-25G

  • 2,179.71CNY

  • Detail

6607-66-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,3-TRIMETHOXYBUTANE

1.2 Other means of identification

Product number -
Other names Butane,1,3,3-trimethoxy

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:6607-66-5 SDS

6607-66-5Downstream Products

6607-66-5Relevant articles and documents

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Killian,Hennion,Nieuwland

, p. 1786 (1934)

-

Thiolation of cycloalkenes C5, C6 by redox-activation of hydrogen sulfide

Shinkar, Elena V.,Kudryavtsev, Daniil A.,Pashchenko, Konstantin P.,Berberova, Nadezhda T.,Okhlobystina, Alexandra V.

, p. 180 - 182 (2017/03/30)

Direct and indirect redox-activation of H2S in the presence of cyclopentene or cyclohexene in MeCN at 25?°C affords the corresponding cycloalkanethiols.

Melamine-(H2SO4)3/melamine-(HNO3)3 instead of H2SO4/HNO3: A safe system for the fast oxidation of thiols and sulfides under solvent-free conditions

Chehardoli, Gholamabbas,Zolfigol, Mohammad Ali

, p. 606 - 612 (2015/11/17)

Melamine reacted with neat sulfuric acid and fuming nitric acid readily to form two new organic solid acids, namely melamine-(H2SO4)3 and melamine-(HNO3)3. Mixture of them acts as a unique powerful system instead of a hazardous H2SO4/HNO3 system for the direct oxidation of thiols. Also, this system can oxidize the sulfides in the presence of a catalytic amount of KBr and few drops of water. This procedure offers advantages such as very low reaction time, simple work-up, excellent yield and matching with some green chemistry protocols.

CERTAIN DIPEPTIDYL PEPTIDASE INHIBITORS

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Paragraph 0184, (2014/06/11)

Provided are certain dipeptidyl peptidase inhibitors, pharmaceutical compositions thereof, and methods of use therefor.

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