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10138-89-3

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10138-89-3 Usage

General Description

1,1,3-Trimethoxybutane is a chemical compound with the formula C7H16O3. This organic compound belongs to the family of alkyl methoxides. It appears as a clear, colorless liquid and is used primarily in the field of organic synthesis as a precursor to other chemicals. Its molecular weight is 148.20 g/mol. It needs to be handled with care as it possesses health hazards such as eye and skin irritation upon contact. It has a moderately high boiling point of 174-176 degrees Celsius and a flash point of 57 degrees Celsius.

Check Digit Verification of cas no

The CAS Registry Mumber 10138-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,3 and 8 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 10138-89:
(7*1)+(6*0)+(5*1)+(4*3)+(3*8)+(2*8)+(1*9)=73
73 % 10 = 3
So 10138-89-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O3/c1-6(8-2)5-7(9-3)10-4/h6-7H,5H2,1-4H3

10138-89-3 Well-known Company Product Price

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  • Aldrich

  • (M13009)  3-Methoxybutyraldehydedimethylacetal  98%

  • 10138-89-3

  • M13009-25G

  • 1,787.76CNY

  • Detail

10138-89-3SDS

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 1,1,3-trimethoxybutane

1.2 Other means of identification

Product number -
Other names Butane, 1,1,3-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:10138-89-3 SDS

10138-89-3Relevant articles and documents

Direct C-4 arylation of crotonaldehyde with arenediazonium tetrafluoroborates

Zaragoza, Florencio,Heinze, Verena

scheme or table, p. 4678 - 4680 (2011/09/20)

Arenediazonium tetrafluoroborates react with crotonaldehyde (2-butenal) in methanol in the presence of catalytic amounts of Pd(OAc)2 to yield mainly 4,4-dimethoxy-1-butenylarenes. In most of the examples studied, small amounts of an isomeric byproduct were formed, presumably 3,3-dimethoxy-1- methylenepropylarenes. Because crotonaldehyde and arenediazonium salts are cheap and readily available, this reaction is a convenient access to protected 4-arylbutenals.

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