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27912-60-3

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27912-60-3 Usage

Appearance

Pale yellow crystalline solid

Usage

a. Reagent in chemical analysis
b. Building block for the synthesis of other organic compounds
c. Determination of nickel ions in solution (forms a complex with nickel, measured spectrophotometrically)
d. Production of pharmaceuticals and dyes

Hazards

a. Can be hazardous if ingested or inhaled
b. Can cause irritation to the skin and eyes

Safety precautions

Handle with care to avoid ingestion, inhalation, or skin/eye contact

Check Digit Verification of cas no

The CAS Registry Mumber 27912-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,9,1 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27912-60:
(7*2)+(6*7)+(5*9)+(4*1)+(3*2)+(2*6)+(1*0)=123
123 % 10 = 3
So 27912-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H12N2O2/c1-7(11-13)9-3-5-10(6-4-9)8(2)12-14/h3-6,11,13H,1-2H3/b9-7-,10-8+

27912-60-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[1-[4-(1-nitrosoethylidene)cyclohexa-2,5-dien-1-ylidene]ethyl]hydroxylamine

1.2 Other means of identification

Product number -
Other names 1,4-diacetylbenzene dioxime

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:27912-60-3 SDS

27912-60-3Upstream product

27912-60-3Relevant articles and documents

Novel photolabile crosslinkers based on O-acyloxime moiety

Suyama, Kanji,Tachi, Hideki

, p. 31506 - 31513 (2015)

Controlled decrosslinking is an attractive technique in the fields of functional materials and polymer recycling. Photo-triggered decrosslinking is especially advantageous for easy remote activation and spatiotemporal control. However, only a few photolab

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