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3457-57-6

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3457-57-6 Usage

Category

Organic nitrite.

Usage

Commonly used as a recreational drug and a room odorizer.

Physical properties

Clear, pale yellow liquid with a fruity, solvent-like odor.

Biological effects

Potent vasodilator, relaxes smooth muscle, and dilates blood vessels, leading to increased blood flow.

Health risks

Potential for abuse and adverse effects, including headaches, dizziness, and lightheadedness.

Legal status

Use is regulated in many countries.

Safety precautions

Flammable, should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 3457-57-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,5 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3457-57:
(6*3)+(5*4)+(4*5)+(3*7)+(2*5)+(1*7)=96
96 % 10 = 6
So 3457-57-6 is a valid CAS Registry Number.

3457-57-6SDS

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 2-methyl-1-nitrobutane

1.2 Other means of identification

Product number -
Other names 1-Nitro-2-methyl-butan

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:3457-57-6 SDS

3457-57-6Downstream Products

3457-57-6Relevant articles and documents

Organocatalytic asymmetric transfer hydrogenation of nitroolefins

Martin, Nolwenn J. A.,Ozores, Lidia,List, Benjamin

, p. 8976 - 8977 (2008/02/10)

We describe a highly efficient and highly enantioselective Hantzsch ester mediated conjugate transfer hydrogenation of β,β-disubstituted nitroolefins that is catalyzed by a Jacobsen-type thiourea catalyst. Copyright

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