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7689-50-1 Usage

Chemical Properties

Crystalline

Check Digit Verification of cas no

The CAS Registry Mumber 7689-50-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,8 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7689-50:
(6*7)+(5*6)+(4*8)+(3*9)+(2*5)+(1*0)=141
141 % 10 = 1
So 7689-50-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO2.ClH/c11-9(12)7-10-6-8-4-2-1-3-5-8;/h1-5,10H,6-7H2,(H,11,12);1H

7689-50-1 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (B3075)  N-Benzylglycine Hydrochloride  >98.0%(HPLC)

  • 7689-50-1

  • 5g

  • 280.00CNY

  • Detail
  • TCI America

  • (B3075)  N-Benzylglycine Hydrochloride  >98.0%(HPLC)

  • 7689-50-1

  • 25g

  • 960.00CNY

  • Detail
  • Alfa Aesar

  • (L15200)  N-Benzylglycine hydrochloride, 98+%   

  • 7689-50-1

  • 5g

  • 404.0CNY

  • Detail
  • Alfa Aesar

  • (L15200)  N-Benzylglycine hydrochloride, 98+%   

  • 7689-50-1

  • 25g

  • 1314.0CNY

  • Detail
  • Alfa Aesar

  • (L15200)  N-Benzylglycine hydrochloride, 98+%   

  • 7689-50-1

  • 100g

  • 5063.0CNY

  • Detail
  • Aldrich

  • (438049)  N-Benzylglycinehydrochloride  98%

  • 7689-50-1

  • 438049-5G

  • CNY

  • Detail
  • Aldrich

  • (438049)  N-Benzylglycinehydrochloride  98%

  • 7689-50-1

  • 438049-25G

  • 1,082.25CNY

  • Detail

7689-50-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzylaminoacetic acid hydrochloride

1.2 Other means of identification

Product number -
Other names 2-(benzylamino)acetic acid,hydrochloride

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:7689-50-1 SDS

7689-50-1Relevant articles and documents

Discovery of seneciobipyrrolidine derivatives for the amelioration of glucose homeostasis disorders through 4E-BP1/Akt/AMPK signaling activation

Che, Jinxin,Ma, Canliang,Lu, Jialiang,Chen, Binhui,Shi, Qiuqiu,Jin, Xinxin,Song, Rui,Xu, Fan,Gan, Lishe,Li, Jingya,Hu, Yongzhou,Dong, Xiaowu

, (2021/11/16)

Modulating the glucose transport in skeletal muscle is a promising strategy for ameliorating glucose homeostasis disorders. However, the complicated mechanisms of glucose transport make it difficult to find compounds therapeutically relevant molecular mechanisms of action, while phenotypic screening is thought to be an alternative approach to mimic the cell state of interest. Here, we report (±)-seneciobipyrrolidine (1a) is first found to enhance glucose uptake in L6 myotubes through phenotype-based screening. Further SAR investigation led to the identfication of compound A27 (EC50 = 2.7 μM). Proteomiic analysis discloses the unique function mechanism of A27 through upregulating the level of the eukaryotic translation initiation factor 4E-binding protein 1 (4E-BP1), subsequently enhancing the Akt and AMPK phosphorylation, thereby promoting the glucose uptake. Chronic oral administration of A27 significantly lowers blood glucose and improves glucose tolerance in db/db mice. This work is new research on seneciobipyrrolidine derivatives, providing a promising avenue for ameliorating glucose homeostasis.

A mild and efficient method for the one-pot monocarboxymethylation of primary amines

Gibbs, Timothy J. K.,Boomhoff, Michael,Tomkinson, Nicholas C. O.

, p. 1573 - 1576 (2008/02/04)

A mild and efficient method for the monocarboxymethylation of primary amines that takes place under aqueous conditions at room temperature is described. Treatment of an aqueous solution of a variety of primary amines with two equivalents of glyoxylic acid

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