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1948-56-7

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1948-56-7 Usage

Uses

Aminoacrylic Acid is an amino acid residue found in peptides. A non-proteinogenic amino acid that aids in the fragmentation of ions derived from polypeptides after collision-induced dissociation.

Definition

ChEBI: A dehydroamino acid that is alanine which has been dehydrogenated to introduce a double bond between positions 2 and 3.

Check Digit Verification of cas no

The CAS Registry Mumber 1948-56-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1948-56:
(6*1)+(5*9)+(4*4)+(3*8)+(2*5)+(1*6)=107
107 % 10 = 7
So 1948-56-7 is a valid CAS Registry Number.
InChI:InChI=1/C3H5NO2/c1-2(4)3(5)6/h1,4H2,(H,5,6)

1948-56-7SDS

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-aminoacrylic acid

1.2 Other means of identification

Product number -
Other names amino acrylic acid

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:1948-56-7 SDS

1948-56-7Upstream product

1948-56-7Downstream Products

1948-56-7Relevant articles and documents

Genetically encoded cleavable protein photo-cross-linker

Lin, Shixian,He, Dan,Long, Teng,Zhang, Shuai,Meng, Rong,Chen, Peng R.

, p. 11860 - 11863 (2014/11/07)

We have developed a genetically encoded, selenium-based cleavable photo-cross-linker that allows for the separation of bait and prey proteins after protein photo-cross-linking. We have further demonstrated the efficient capture of the in situ generated selenenic acid on the cleaved prey proteins. Our strategy involves tagging the selenenic acid with an alkyne-containing dimethoxyaniline molecule and subsequently labeling with an azide-bearing fluorophore or biotin probe. This cleavage-and-capture after protein photo-cross-linking strategy allows for the efficient capture of prey proteins that are readily accessible by two-dimensional gel-based proteomics and mass spectrometry analysis.

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