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84508-51-0

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84508-51-0 Usage

Uses

2-Bromoethanol-13C2, is the labeled analogue of 2-Bromoethanol (B684735), an widely used intermediate in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 84508-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,0 and 8 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84508-51:
(7*8)+(6*4)+(5*5)+(4*0)+(3*8)+(2*5)+(1*1)=140
140 % 10 = 0
So 84508-51-0 is a valid CAS Registry Number.

84508-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromoethanol

1.2 Other means of identification

Product number -
Other names Ethylene-13C2 bromohydrin

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:84508-51-0 SDS

84508-51-0Upstream product

84508-51-0Downstream Products

84508-51-0Relevant articles and documents

Synthesis of stable-isotope-labeled N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide and N-(3-dimethylaminopropyl)-N′-ethylurea

Cao, Kai,Brailsford, John A.,Bonacorsi, Samuel J.

, p. 526 - 530 (2020)

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide (EDC) is a carbodiimide coupling reagent commonly used for the preparation of amides from carboxylic acids and amines. Because of initial concerns regarding the genotoxicity of EDC and its use in GMP syntheses at Bristol Myers Squibb, the quantitation of residual EDC and its by-product N-(3-dimethylaminopropyl)-N′-ethylurea (EDU) by liquid chromatography–mass spectrometry (LCMS) impurity analysis was required. These analyses required the use of stable-isotope-labeled EDC and EDU to serve as internal standards. To meet this need, stable-isotope-labeled EDC 9 and EDU 10 were prepared from [1,2-13C2] ethylene glycol and [13C,15N] potassium cyanide in overall yields of 6% and 8%, respectively.

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