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51827-14-6

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51827-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51827-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,8,2 and 7 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 51827-14:
(7*5)+(6*1)+(5*8)+(4*2)+(3*7)+(2*1)+(1*4)=116
116 % 10 = 6
So 51827-14-6 is a valid CAS Registry Number.

51827-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Phenylmethoxy)carbonyl]-L-valyl-L-proline methyl ester

1.2 Other means of identification

Product number -
Other names Cbz-L-valine-L-proline methyl ester

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:51827-14-6 SDS

51827-14-6Relevant articles and documents

MALT1 INHIBITORS AND USES THEREOF

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Paragraph 00324; 00325; 00328, (2019/08/15)

Provided herein are compounds of Formula (I) and pharmaceutical compositions thereof, which may be useful as MALT1 inhibitors. Also provided are for the treatment of proliferative disorders (e.g., cancer (e.g., non-Hodgkin' s lymphoma, diffuse large B-cell lymphoma, MALT lymphoma), benign neoplasm, a disease associated with angiogenesis,an autoimmune disease, an inflammatory disease, an autoinflammatory disease) by administering a compound of Formula (I).

Expeditious amide-forming reactions using thiol esters

Kurosu, Michio

, p. 591 - 594 (2007/10/03)

The reaction of a 2-pyridylthiol ester with a dimethylaluminum amide leads to the rapid formation of the corresponding amide. The tolylthiol esters can be activated with silver trifluoroacetate and coupled even with poorly reactive amino compounds. (C) 20

Rapid, one-pot synthesis of urethane-protected tripeptides

Zhu, Yun-Fei,Fuller, William D.

, p. 807 - 810 (2007/10/02)

Urethane-protected tripeptides are synthesized in solution, without isolation of purification of intermediates, using urethane-protected N-carboxyanhydrides as coupling reagents and hydrogenation for removal of N-protection.

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