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53984-12-6

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53984-12-6 Usage

Physical Properties

Color: Colorless
Odor: Strong, sweet
State: Liquid
Solubility: Insoluble in water

Applications

Intermediate in pharmaceutical synthesis
Intermediate in agrochemical synthesis
Intermediate in organic compound synthesis
Used in dye production
Used in plastic production
Utilized in the production of other industrial products

Safety Considerations

Toxicity: Handle with care
Potential Irritants: Skin, eyes, respiratory system

Check Digit Verification of cas no

The CAS Registry Mumber 53984-12-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,8 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53984-12:
(7*5)+(6*3)+(5*9)+(4*8)+(3*4)+(2*1)+(1*2)=146
146 % 10 = 6
So 53984-12-6 is a valid CAS Registry Number.

53984-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-5-nitro-6-styrylbenzo[d][1,3]dioxole

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:53984-12-6 SDS

53984-12-6Relevant articles and documents

N, N′-dioxide-Cu(OTf)2 complex catalyzed highly enantioselective amination reaction of N-acetyl enamide

Chang, Lu,Kuang, Yulong,Qin, Bo,Zhou, Xin,Liu, Xiaohua,Lin, Lili,Feng, Xiaoming

supporting information; experimental part, p. 2214 - 2217 (2010/08/06)

The N,N′-dioxide-Cu(OTf)2 complexes were applied in the asymmetric amination reaction of N-acetyl enamides with dialkyl azodicarboxylate, giving the corresponding products in good yields with high enantioselectivities (up to 91% ee). Precursors of vicinal diamine were readily obtained with excellent diastereoselectivities (>95:5) by NaBH4 reduction.

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