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1604-35-9

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1604-35-9 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 1604-35-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,0 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1604-35:
(6*1)+(5*6)+(4*0)+(3*4)+(2*3)+(1*5)=59
59 % 10 = 9
So 1604-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H28O/c1-6-15(5,16)12-8-11-14(4)10-7-9-13(2)3/h1,13-14,16H,7-12H2,2-5H3

1604-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,7,11-trimethyldodec-1-yn-3-ol

1.2 Other means of identification

Product number -
Other names (3S,7R)-3,7,11-trimethyldodec-1-yn-3-ol

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:1604-35-9 SDS

1604-35-9Relevant articles and documents

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Ustynyuk et al.

, (1972)

-

Acetylene method (by machine translation)

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Paragraph 0054-0056, (2019/11/29)

In the presence of a catalyst alkoxide or an amino N,N - salt, the saturated or unsaturated ketone or aldehyde compound is subjected to acetylene hydrogenation to obtain the corresponding alkynol compound, and has the advantages of moderate reaction rate, mild reaction, easy control, easy separation of the product, recyclable solvent and the like. (by machine translation)

(6R,10R)-6,10,14-TRIMETYLPENTADECAN-2-ONE PREPARED FROM (R)-3,7-DIMETYLOCT-6-ENAL

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Page/Page column 45, (2014/07/08)

The present invention relates to a process of manufacturing (6R,10R)-6,10,14-trimetylpentadecan-2-one in a multistep synthesis from (R)-3,7-dimethyloct-6-enal. The process is very advantageous in that it forms in an efficient way the desired chiral product from a mixture of stereoisomers of the starting product.

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