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29865-53-0

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29865-53-0 Usage

Physical State

Pale yellow liquid
A liquid substance with a pale yellow color.

Odor

Sweet, floral
Possessing a pleasant, sweet, and flower-like scent.

Applications

Fragrances and flavoring agents
Commonly used in products like shampoos, soaps, and perfumes for its appealing aroma.
6. Antimicrobial properties
Exhibits the ability to inhibit or kill microorganisms, making it useful in personal care and cosmetic products for maintaining cleanliness and preventing infections.
7. Antioxidant properties
Helps prevent the oxidation of other compounds, potentially preserving the quality and shelf life of products it is added to.

Health benefits

Potential health benefits
The antimicrobial and antioxidant properties may contribute to positive health effects when used in personal care and cosmetic products.

Check Digit Verification of cas no

The CAS Registry Mumber 29865-53-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,8,6 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29865-53:
(7*2)+(6*9)+(5*8)+(4*6)+(3*5)+(2*5)+(1*3)=160
160 % 10 = 0
So 29865-53-0 is a valid CAS Registry Number.

29865-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-3-(2-nitropropyl)benzene

1.2 Other means of identification

Product number -
Other names -

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:29865-53-0 SDS

29865-53-0Downstream Products

29865-53-0Relevant articles and documents

Enantioselective hydrogenation of α,β-disubstituted nitroalkenes

Li, Shengkun,Huang, Kexuan,Zhang, Xumu

supporting information, p. 8878 - 8881 (2014/08/05)

The first highly chemo- and enantioselective hydrogenation of α,β-disubstituted nitroalkenes was accomplished with rhodium/JosiPhos-J2 as a catalyst, with the yield and enantioselectivity of up to 95% and 94%, respectively. The α-chiral nitroalkanes will provide an entry to valuable chiral amphetamines which are otherwise not so easily accessed. This journal is the Partner Organisations 2014.

REDUCTION OF AROMATIC NITROALKENES WITH BAKER'S YEAST

Takeshita, Mitsuhiro,Yoshida, Sachiko,Kohno, Yoichiro

, p. 553 - 562 (2007/10/02)

Aromatic nitroalkenes were reduced chemoselectively with baker's yeast to give the corresponding nitroalkanes.

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